geneid | 57597 |
---|---|
ensemblid | ENSG00000266074.11 |
hgncid | 29279 |
symbol | BAHCC1 |
name | BAH domain and coiled-coil containing 1 |
refseq_nuc | NM_001377448.1 |
refseq_prot | NP_001364377.1 |
ensembl_nuc | ENST00000675386.2 |
ensembl_prot | ENSP00000502710.1 |
mane_status | MANE Select |
chr | chr17 |
start | 81395457 |
end | 81466331 |
strand | + |
ver | v1.2 |
region | chr17:81395457-81466331 |
region5000 | chr17:81390457-81471331 |
regionname0 | BAHCC1_chr17_81395457_81466331 |
regionname5000 | BAHCC1_chr17_81390457_81471331 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2608 | 74 | 17 | 14 | 36 | 4 | 2 | 25 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002 | 0/0 | 2608 | 73 | 14 | 6 | 43 | 1 | 9 | 25 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003 | 0/0 | 2608 | 46 | 6 | 14 | 21 | 0 | 5 | 13 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004 | 0/0 | 2608 | 34 | 13 | 13 | 0 | 3 | 5 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005 | 0/0 | 2608 | 14 | 0 | 2 | 8 | 0 | 4 | 6 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0006 | 0/0 | 2608 | 10 | 2 | 7 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0007 | 0/0 | 2608 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008 | 0/0 | 2608 | 5 | 1 | 0 | 1 | 0 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0009 | 0/0 | 2608 | 5 | 0 | 2 | 0 | 0 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0010 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0011 | 0/0 | 2608 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0012 | 0/0 | 2608 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0013 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0014 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0015 | 0/0 | 2608 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0016 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0017 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0018 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0019 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0020 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0021 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0022 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0023 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0024 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0025 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0026 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0027 | 0/0 | 2618 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0028 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0029 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0030 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0031 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0032 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0033 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0034 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0035 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0036 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0037 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0038 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0039 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0040 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0041 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0042 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0043 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0044 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0045 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0046 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0047 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0048 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0049 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0050 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0051 | 1/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0052 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0053 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0054 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0055 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0056 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0057 | 0/0 | 2612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 7827 | 59 | 13 | 6 | 32 | 1 | 7 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0002 | 0/0 | 7827 | 42 | 6 | 12 | 19 | 0 | 5 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0003 | 0/0 | 7827 | 28 | 0 | 4 | 21 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0004 | 0/0 | 7827 | 27 | 11 | 11 | 0 | 3 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0005 | 0/0 | 7827 | 9 | 0 | 2 | 4 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0006 | 0/0 | 7827 | 7 | 0 | 6 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0007 | 0/1 | 7827 | 7 | 6 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0008 | 0/0 | 7827 | 6 | 5 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0009 | 0/0 | 7827 | 6 | 3 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0010 | 0/0 | 7827 | 6 | 1 | 2 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0011 | 0/0 | 7827 | 5 | 1 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0012 | 0/0 | 7827 | 5 | 1 | 2 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0013 | 0/0 | 7827 | 4 | 0 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0014 | 0/0 | 7827 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0015 | 0/0 | 7827 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0016 | 0/0 | 7827 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0017 | 0/0 | 7827 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0018 | 0/0 | 7827 | 3 | 0 | 2 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0019 | 0/0 | 7827 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0020 | 0/0 | 7827 | 3 | 2 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0021 | 0/0 | 7827 | 3 | 1 | 1 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0022 | 0/0 | 7827 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0023 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0024 | 0/0 | 7827 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0025 | 0/0 | 7827 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0026 | 0/0 | 7827 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0027 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0028 | 0/0 | 7827 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0029 | 0/0 | 7827 | 2 | 1 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0030 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0031 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0032 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0033 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0034 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0035 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0036 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0037 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0038 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0039 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0040 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0041 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0042 | 1/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0043 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0044 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0045 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0046 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0047 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0048 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0049 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0050 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0051 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0052 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0053 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0054 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0055 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0056 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0057 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0058 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0059 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0060 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0061 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0062 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0063 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0064 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0065 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0066 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0067 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0068 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0069 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0070 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0071 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0072 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0073 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0074 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0075 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0076 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0077 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0078 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0079 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0080 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0081 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0082 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0083 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0084 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0085 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0086 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0087 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0088 | 0/0 | 7857 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0089 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0090 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0091 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0092 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0093 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0094 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0095 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0096 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0097 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0098 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0099 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0100 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0101 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0102 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0103 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0104 | 0/0 | 7839 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0105 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0106 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
c0107 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2900 | 128 | 25 | 25 | 66 | 1 | 11 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0002 | 0/1 | 2900 | 62 | 19 | 27 | 1 | 5 | 9 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0003 | 1/0 | 2900 | 45 | 0 | 5 | 35 | 3 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0004 | 0/0 | 2900 | 26 | 7 | 6 | 5 | 1 | 7 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0005 | 0/0 | 2900 | 8 | 0 | 0 | 6 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0006 | 0/0 | 2900 | 6 | 0 | 3 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0007 | 0/0 | 2900 | 6 | 3 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0008 | 0/0 | 2900 | 6 | 0 | 2 | 4 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0009 | 0/0 | 2900 | 4 | 4 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0010 | 0/0 | 2900 | 4 | 3 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0011 | 0/0 | 2900 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0012 | 0/0 | 2900 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0013 | 0/0 | 2900 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0014 | 0/0 | 2900 | 2 | 1 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0015 | 0/0 | 2900 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0016 | 0/0 | 2900 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0017 | 0/0 | 2900 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0018 | 0/0 | 2900 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0019 | 0/0 | 2900 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0020 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0021 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0022 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0023 | 0/0 | 2900 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0024 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0025 | 0/0 | 2900 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0026 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0027 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0028 | 0/0 | 2900 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0029 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0030 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0031 | 0/0 | 2900 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0032 | 0/0 | 2900 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0033 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0034 | 0/0 | 2900 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0035 | 0/0 | 2900 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0036 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0037 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
t0038 | 0/0 | 2900 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003 | 0/0 | 7827 | 28 | 0 | 4 | 21 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0007 | 0/1 | 7827 | 7 | 6 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009 | 0/0 | 7827 | 6 | 3 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0010 | 0/0 | 7827 | 6 | 1 | 2 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0012 | 0/0 | 7827 | 5 | 1 | 2 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0019 | 0/0 | 7827 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0021 | 0/0 | 7827 | 3 | 1 | 1 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0025 | 0/0 | 7827 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0026 | 0/0 | 7827 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0032 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0051 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0068 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0069 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0085 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0086 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0092 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0093 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0094 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0099 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0101 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0103 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001 | 0/0 | 7827 | 59 | 13 | 6 | 32 | 1 | 7 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0016 | 0/0 | 7827 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0044 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0052 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0055 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0056 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0057 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0062 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0063 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0072 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0074 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0076 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0081 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0002 | 0/0 | 7827 | 42 | 6 | 12 | 19 | 0 | 5 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0018 | 0/0 | 7827 | 3 | 0 | 2 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0064 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0004 | 0/0 | 7827 | 27 | 11 | 11 | 0 | 3 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0011 | 0/0 | 7827 | 5 | 1 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0035 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0037 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0005 | 0/0 | 7827 | 9 | 0 | 2 | 4 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0028 | 0/0 | 7827 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0065 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0066 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0096 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0006c0006 | 0/0 | 7827 | 7 | 0 | 6 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0006c0020 | 0/0 | 7827 | 3 | 2 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0007c0008 | 0/0 | 7827 | 6 | 5 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0007c0048 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0024 | 0/0 | 7827 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0029 | 0/0 | 7827 | 2 | 1 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0073 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0009c0013 | 0/0 | 7827 | 4 | 0 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0009c0087 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0010c0031 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0010c0102 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0011c0015 | 0/0 | 7827 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0012c0017 | 0/0 | 7827 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0013c0027 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0013c0097 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0014c0022 | 0/0 | 7827 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0015c0014 | 0/0 | 7827 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0016c0030 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0017c0023 | 0/0 | 7827 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0018c0039 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0018c0106 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0019c0036 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0019c0105 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0020c0049 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0021c0079 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0022c0078 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0023c0084 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0024c0082 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0025c0107 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0026c0083 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0027c0088 | 0/0 | 7857 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0028c0089 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0029c0070 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0030c0090 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0031c0091 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0032c0071 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0033c0067 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0034c0033 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0035c0095 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0036c0061 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0037c0060 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0038c0059 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0039c0058 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0040c0054 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0041c0053 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0042c0075 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0043c0077 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0044c0050 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0045c0080 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0046c0047 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0047c0046 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0048c0045 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0049c0098 | 0/0 | 7827 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0050c0043 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0051c0042 | 1/0 | 7827 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0052c0038 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0053c0040 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0054c0041 | 0/0 | 7827 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0055c0034 | 0/0 | 7827 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0056c0100 | 0/0 | 7827 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0057c0104 | 0/0 | 7839 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003t0003 | 0/0 | 10726 | 27 | 0 | 3 | 21 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0003t0010 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0007t0002 | 0/1 | 10726 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0007t0009 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0007t0015 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0007t0016 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0007t0033 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009t0004 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009t0006 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009t0024 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009t0025 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009t0030 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0009t0037 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0010t0001 | 0/0 | 10726 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0010t0004 | 0/0 | 10726 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0010t0009 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0012t0002 | 0/0 | 10726 | 5 | 1 | 2 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0019t0003 | 0/0 | 10726 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0021t0002 | 0/0 | 10726 | 3 | 1 | 1 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0025t0003 | 0/0 | 10726 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0026t0003 | 0/0 | 10726 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0032t0003 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0051t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0068t0008 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0069t0007 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0085t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0086t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0092t0004 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0093t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0094t0009 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0099t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0101t0010 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0001c0103t0026 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0001 | 0/0 | 10726 | 47 | 13 | 2 | 30 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0002 | 0/0 | 10726 | 6 | 0 | 2 | 1 | 1 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0005 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0006 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0007 | 0/0 | 10726 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0018 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0001t0031 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0016t0001 | 0/0 | 10726 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0044t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0052t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0055t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0056t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0057t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0062t0007 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0063t0020 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0072t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0074t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0076t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0002c0081t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0002t0001 | 0/0 | 10726 | 24 | 1 | 9 | 14 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0002t0004 | 0/0 | 10726 | 13 | 2 | 2 | 4 | 0 | 5 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0002t0013 | 0/0 | 10726 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0002t0028 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0002t0035 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0018t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0018t0002 | 0/0 | 10726 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0003c0064t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0004t0002 | 0/0 | 10726 | 24 | 9 | 11 | 0 | 2 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0004t0014 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0004t0022 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0004t0029 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0011t0002 | 0/0 | 10726 | 3 | 1 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0011t0004 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0011t0023 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0035t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0004c0037t0014 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0005t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0005t0008 | 0/0 | 10726 | 5 | 0 | 2 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0005t0012 | 0/0 | 10726 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0028t0001 | 0/0 | 10726 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0065t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0066t0034 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0005c0096t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0006c0006t0001 | 0/0 | 10726 | 4 | 0 | 3 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0006c0006t0002 | 0/0 | 10726 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0006c0020t0002 | 0/0 | 10726 | 3 | 2 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0007c0008t0001 | 0/0 | 10726 | 5 | 4 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0007c0008t0004 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0007c0048t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0024t0001 | 0/0 | 10726 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0029t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0029t0021 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0008c0073t0002 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0009c0013t0006 | 0/0 | 10726 | 4 | 0 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0009c0087t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0010c0031t0004 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0010c0102t0004 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0011c0015t0001 | 0/0 | 10726 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0012c0017t0001 | 0/0 | 10726 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0013c0027t0001 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0013c0097t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0014c0022t0011 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0014c0022t0036 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0015c0014t0001 | 0/0 | 10726 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0016c0030t0007 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0017c0023t0015 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0017c0023t0038 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0018c0039t0011 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0018c0106t0010 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0019c0036t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0019c0105t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0020c0049t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0021c0079t0003 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0022c0078t0005 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0023c0084t0003 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0024c0082t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0025c0107t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0026c0083t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0027c0088t0004 | 0/0 | 10756 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0028c0089t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0029c0070t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0030c0090t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0031c0091t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0032c0071t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0033c0067t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0034c0033t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0035c0095t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0036c0061t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0037c0060t0032 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0038c0059t0002 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0039c0058t0017 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0040c0054t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0041c0053t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0042c0075t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0043c0077t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0044c0050t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0045c0080t0004 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0046c0047t0027 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0047c0046t0004 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0048c0045t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0049c0098t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0050c0043t0004 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0051c0042t0003 | 1/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0052c0038t0002 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0053c0040t0002 | 0/0 | 10714 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0054c0041t0019 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0055c0034t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0056c0100t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
a0057c0104t0010 | 0/0 | 10738 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | copy fasta | chr17 | 81390457 | 81471331 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0003t0010g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0002g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0016g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0016g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0007t0033g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0009t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0009t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0009t0024g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0009t0025g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0009t0030g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0009t0037g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0010t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0010t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0010t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0010t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0010t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0010t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0012t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0012t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0012t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0012t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0012t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0019t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0019t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0019t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0021t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0021t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0021t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0025t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0025t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0026t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0026t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0032t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0051t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0068t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0069t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0085t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0086t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0092t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0093t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0094t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0099t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0101t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0001c0103t0026g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0018g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0001t0031g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0016t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0016t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0016t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0044t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0052t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0055t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0056t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0057t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0062t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0063t0020g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0072t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0074t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0076t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0002c0081t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0028g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0002t0035g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0018t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0018t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0018t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0003c0064t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0014g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0022g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0004t0029g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0011t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0011t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0011t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0011t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0011t0023g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0035t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0004c0037t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0008g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0008g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0012g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0005t0012g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0028t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0028t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0065t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0066t0034g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0005c0096t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0006t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0020t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0020t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0006c0020t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0008t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0008t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0008t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0008t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0008t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0008t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0007c0048t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0008c0024t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0008c0024t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0008c0029t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0008c0029t0021g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0008c0073t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0009c0013t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0009c0013t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0009c0013t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0009c0013t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0009c0087t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0010c0031t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0010c0031t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0010c0102t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0011c0015t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0011c0015t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0011c0015t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0012c0017t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0012c0017t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0012c0017t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0013c0027t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0013c0027t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0013c0097t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0014c0022t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0014c0022t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0014c0022t0036g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0015c0014t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0015c0014t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0016c0030t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0016c0030t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0017c0023t0015g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0017c0023t0038g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0018c0039t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0018c0106t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0019c0036t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0019c0105t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0020c0049t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0021c0079t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0022c0078t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0023c0084t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0024c0082t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0025c0107t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0026c0083t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0027c0088t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0028c0089t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0029c0070t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0030c0090t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0031c0091t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0032c0071t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0033c0067t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0034c0033t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0035c0095t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0036c0061t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0037c0060t0032g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0038c0059t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0039c0058t0017g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0040c0054t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0041c0053t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0042c0075t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0043c0077t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0044c0050t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0045c0080t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0046c0047t0027g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0047c0046t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0048c0045t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0049c0098t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0050c0043t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0051c0042t0003g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0052c0038t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0053c0040t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0054c0041t0019g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0055c0034t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0056c0100t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
a0057c0104t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0052 | c0038 | t0002 | g0144 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00099 | hp2 | a0001 | c0021 | t0002 | g0077 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00140 | hp1 | a0002 | c0001 | t0002 | g0142 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00140 | hp2 | a0004 | c0004 | t0002 | g0219 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0068 | EUR | FIN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00323 | hp2 | a0004 | c0004 | t0014 | g0190 | EUR | FIN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00408 | hp1 | a0001 | c0003 | t0003 | g0293 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0203 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00423 | hp1 | a0002 | c0074 | t0001 | g0054 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00423 | hp2 | a0003 | c0002 | t0001 | g0124 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0037 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00438 | hp2 | a0005 | c0005 | t0008 | g0188 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0304 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00544 | hp2 | a0003 | c0002 | t0004 | g0123 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0292 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00609 | hp2 | a0002 | c0044 | t0001 | g0164 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00639 | hp1 | a0015 | c0014 | t0001 | g0243 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00639 | hp2 | a0001 | c0003 | t0003 | g0231 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00642 | hp1 | a0004 | c0004 | t0002 | g0241 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00642 | hp2 | a0003 | c0018 | t0002 | g0143 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00673 | hp1 | a0001 | c0003 | t0003 | g0046 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00673 | hp2 | a0002 | c0056 | t0001 | g0038 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00733 | hp1 | a0035 | c0095 | t0002 | g0146 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00733 | hp2 | a0004 | c0004 | t0002 | g0093 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00735 | hp1 | a0004 | c0004 | t0002 | g0158 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00735 | hp2 | a0002 | c0001 | t0002 | g0012 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00738 | hp1 | a0004 | c0004 | t0002 | g0149 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00738 | hp2 | a0055 | c0034 | t0002 | g0216 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00741 | hp1 | a0003 | c0002 | t0001 | g0101 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG00741 | hp2 | a0004 | c0035 | t0002 | g0215 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01069 | hp1 | a0006 | c0006 | t0002 | g0153 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01069 | hp2 | a0005 | c0005 | t0008 | g0297 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01070 | hp1 | a0001 | c0003 | t0010 | g0211 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01070 | hp2 | a0003 | c0002 | t0001 | g0002 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01071 | hp1 | a0003 | c0002 | t0001 | g0002 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01071 | hp2 | a0006 | c0006 | t0002 | g0154 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01074 | hp1 | a0004 | c0011 | t0002 | g0162 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01074 | hp2 | a0006 | c0020 | t0002 | g0325 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01106 | hp1 | a0004 | c0004 | t0002 | g0092 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01106 | hp2 | a0012 | c0017 | t0001 | g0228 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01109 | hp1 | a0021 | c0079 | t0003 | g0192 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01109 | hp2 | a0003 | c0002 | t0001 | g0100 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01167 | hp1 | a0004 | c0004 | t0002 | g0240 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01167 | hp2 | a0003 | c0002 | t0004 | g0170 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01168 | hp1 | a0004 | c0004 | t0002 | g0010 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01168 | hp2 | a0015 | c0014 | t0001 | g0001 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01169 | hp1 | a0015 | c0014 | t0001 | g0001 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01169 | hp2 | a0003 | c0002 | t0004 | g0171 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0233 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01175 | hp2 | a0026 | c0083 | t0001 | g0099 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01192 | hp1 | a0004 | c0004 | t0002 | g0167 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01192 | hp2 | a0009 | c0013 | t0006 | g0072 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01243 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01243 | hp2 | a0007 | c0008 | t0001 | g0309 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01255 | hp1 | a0004 | c0004 | t0002 | g0266 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01255 | hp2 | a0001 | c0009 | t0004 | g0117 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01261 | hp1 | a0001 | c0009 | t0006 | g0134 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01261 | hp2 | a0001 | c0009 | t0025 | g0252 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01346 | hp1 | a0012 | c0017 | t0001 | g0180 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01346 | hp2 | a0001 | c0012 | t0002 | g0159 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01358 | hp1 | a0002 | c0001 | t0031 | g0196 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01358 | hp2 | a0006 | c0006 | t0001 | g0150 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01361 | hp1 | a0003 | c0018 | t0002 | g0210 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0141 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01433 | hp1 | a0003 | c0002 | t0001 | g0098 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01433 | hp2 | a0033 | c0067 | t0001 | g0305 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01496 | hp1 | a0001 | c0021 | t0002 | g0114 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01496 | hp2 | a0002 | c0001 | t0002 | g0074 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01515 | hp1 | a0001 | c0003 | t0003 | g0186 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01515 | hp2 | a0054 | c0041 | t0019 | g0013 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01516 | hp1 | a0045 | c0080 | t0004 | g0128 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01516 | hp2 | a0001 | c0003 | t0003 | g0184 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0320 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01884 | hp2 | a0048 | c0045 | t0001 | g0254 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01891 | hp1 | a0007 | c0008 | t0001 | g0021 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01891 | hp2 | a0004 | c0004 | t0002 | g0271 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01928 | hp1 | a0003 | c0002 | t0001 | g0105 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01928 | hp2 | a0009 | c0087 | t0002 | g0089 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01934 | hp1 | a0005 | c0005 | t0008 | g0298 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01934 | hp2 | a0004 | c0004 | t0002 | g0218 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01943 | hp1 | a0001 | c0092 | t0004 | g0227 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01943 | hp2 | a0001 | c0003 | t0003 | g0067 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01952 | hp1 | a0003 | c0002 | t0001 | g0106 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0113 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01975 | hp1 | a0012 | c0017 | t0001 | g0301 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01975 | hp2 | a0043 | c0077 | t0001 | g0094 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01978 | hp1 | a0006 | c0006 | t0002 | g0155 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01978 | hp2 | a0001 | c0010 | t0004 | g0121 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01981 | hp1 | a0001 | c0032 | t0003 | g0232 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01981 | hp2 | a0003 | c0002 | t0001 | g0075 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02004 | hp1 | a0001 | c0010 | t0004 | g0296 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02004 | hp2 | a0003 | c0002 | t0001 | g0111 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02015 | hp1 | a0001 | c0010 | t0001 | g0082 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02015 | hp2 | a0001 | c0025 | t0003 | g0212 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0282 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02027 | hp2 | a0003 | c0002 | t0001 | g0057 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02055 | hp1 | a0001 | c0009 | t0030 | g0263 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02055 | hp2 | a0004 | c0037 | t0014 | g0256 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02056 | hp2 | a0020 | c0049 | t0003 | g0079 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02071 | hp2 | a0003 | c0002 | t0001 | g0183 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02074 | hp1 | a0003 | c0002 | t0001 | g0107 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02074 | hp2 | a0001 | c0099 | t0003 | g0051 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02080 | hp1 | a0001 | c0003 | t0003 | g0050 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02080 | hp2 | a0003 | c0002 | t0001 | g0213 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02083 | hp1 | a0001 | c0051 | t0001 | g0288 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02083 | hp2 | a0005 | c0028 | t0001 | g0069 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02129 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02129 | hp2 | a0002 | c0016 | t0001 | g0316 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0302 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02132 | hp2 | a0003 | c0002 | t0035 | g0197 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02135 | hp1 | a0002 | c0016 | t0001 | g0181 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02135 | hp2 | a0002 | c0001 | t0002 | g0130 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02155 | hp1 | a0002 | c0001 | t0018 | g0040 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02155 | hp2 | a0001 | c0003 | t0003 | g0047 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02165 | hp1 | a0008 | c0029 | t0005 | g0066 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02165 | hp2 | a0002 | c0001 | t0001 | g0081 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02257 | hp1 | a0002 | c0001 | t0001 | g0157 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02257 | hp2 | a0003 | c0002 | t0013 | g0173 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02258 | hp1 | a0053 | c0040 | t0002 | g0268 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02258 | hp2 | a0010 | c0102 | t0004 | g0017 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02273 | hp1 | a0003 | c0002 | t0028 | g0299 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02273 | hp2 | a0006 | c0006 | t0001 | g0151 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02280 | hp1 | a0002 | c0001 | t0001 | g0242 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02280 | hp2 | a0004 | c0004 | t0002 | g0003 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02300 | hp1 | a0002 | c0001 | t0006 | g0148 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02300 | hp2 | a0028 | c0089 | t0001 | g0261 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02451 | hp1 | a0001 | c0069 | t0007 | g0253 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02451 | hp2 | a0001 | c0012 | t0002 | g0058 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02523 | hp1 | a0029 | c0070 | t0003 | g0116 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02523 | hp2 | a0034 | c0033 | t0001 | g0178 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02615 | hp1 | a0001 | c0103 | t0026 | g0245 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02615 | hp2 | a0013 | c0097 | t0001 | g0235 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02622 | hp1 | a0001 | c0010 | t0009 | g0185 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02622 | hp2 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02630 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02630 | hp2 | a0001 | c0007 | t0016 | g0161 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02647 | hp1 | a0013 | c0027 | t0001 | g0025 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02647 | hp2 | a0014 | c0022 | t0011 | g0322 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02683 | hp1 | a0008 | c0073 | t0002 | g0193 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02683 | hp2 | a0002 | c0001 | t0002 | g0177 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02698 | hp1 | a0002 | c0081 | t0001 | g0043 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02698 | hp2 | a0004 | c0004 | t0002 | g0127 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02717 | hp1 | a0047 | c0046 | t0004 | g0273 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02717 | hp2 | a0017 | c0023 | t0015 | g0277 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02723 | hp1 | a0014 | c0022 | t0011 | g0323 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02723 | hp2 | a0002 | c0001 | t0001 | g0276 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02735 | hp1 | a0011 | c0015 | t0001 | g0118 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02735 | hp2 | a0004 | c0011 | t0002 | g0120 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02738 | hp1 | a0003 | c0002 | t0004 | g0194 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02738 | hp2 | a0004 | c0011 | t0023 | g0041 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02809 | hp1 | a0002 | c0063 | t0020 | g0251 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02809 | hp2 | a0007 | c0008 | t0001 | g0312 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02818 | hp1 | a0019 | c0036 | t0001 | g0019 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02818 | hp2 | a0001 | c0007 | t0033 | g0135 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02886 | hp1 | a0002 | c0001 | t0001 | g0274 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02886 | hp2 | a0003 | c0002 | t0013 | g0168 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02895 | hp1 | a0003 | c0002 | t0004 | g0172 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02895 | hp2 | a0010 | c0031 | t0004 | g0015 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02922 | hp1 | a0002 | c0001 | t0001 | g0327 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02922 | hp2 | a0007 | c0048 | t0002 | g0308 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02965 | hp1 | a0002 | c0001 | t0001 | g0324 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02965 | hp2 | a0007 | c0008 | t0001 | g0257 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0326 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02976 | hp2 | a0017 | c0023 | t0038 | g0027 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03017 | hp1 | a0002 | c0001 | t0002 | g0132 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03017 | hp2 | a0002 | c0001 | t0007 | g0090 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03098 | hp1 | a0001 | c0021 | t0002 | g0262 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03098 | hp2 | a0004 | c0004 | t0002 | g0272 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03130 | hp1 | a0001 | c0007 | t0009 | g0260 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03130 | hp2 | a0004 | c0011 | t0002 | g0023 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03139 | hp1 | a0002 | c0001 | t0001 | g0174 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03139 | hp2 | a0016 | c0030 | t0007 | g0032 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03195 | hp1 | a0007 | c0008 | t0001 | g0005 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03195 | hp2 | a0004 | c0004 | t0022 | g0139 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03209 | hp1 | a0030 | c0090 | t0002 | g0265 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03209 | hp2 | a0004 | c0004 | t0002 | g0269 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03239 | hp1 | a0002 | c0001 | t0001 | g0136 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03239 | hp2 | a0005 | c0005 | t0012 | g0204 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03453 | hp1 | a0008 | c0029 | t0021 | g0311 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03453 | hp2 | a0004 | c0004 | t0002 | g0222 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03486 | hp1 | a0001 | c0007 | t0009 | g0014 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03486 | hp2 | a0003 | c0002 | t0004 | g0310 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03490 | hp1 | a0009 | c0013 | t0006 | g0029 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03490 | hp2 | a0023 | c0084 | t0003 | g0129 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03491 | hp1 | a0005 | c0005 | t0012 | g0207 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03491 | hp2 | a0027 | c0088 | t0004 | g0165 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03492 | hp1 | a0005 | c0005 | t0012 | g0206 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03492 | hp2 | a0009 | c0013 | t0006 | g0140 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03516 | hp1 | a0046 | c0047 | t0027 | g0264 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03516 | hp2 | a0003 | c0002 | t0013 | g0024 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03540 | hp1 | a0006 | c0020 | t0002 | g0022 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03540 | hp2 | a0001 | c0101 | t0010 | g0020 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03579 | hp1 | a0001 | c0094 | t0009 | g0016 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03579 | hp2 | a0025 | c0107 | t0002 | g0250 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03654 | hp1 | a0002 | c0001 | t0005 | g0064 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03654 | hp2 | a0038 | c0059 | t0002 | g0008 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03669 | hp1 | a0009 | c0013 | t0006 | g0163 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03669 | hp2 | a0011 | c0015 | t0001 | g0119 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0030 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03831 | hp2 | a0008 | c0024 | t0001 | g0175 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03834 | hp1 | a0004 | c0011 | t0004 | g0071 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03834 | hp2 | a0040 | c0054 | t0001 | g0126 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03927 | hp1 | a0024 | c0082 | t0001 | g0236 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03927 | hp2 | a0004 | c0004 | t0002 | g0061 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03942 | hp1 | a0003 | c0002 | t0004 | g0205 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03942 | hp2 | a0005 | c0066 | t0034 | g0313 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04115 | hp1 | a0001 | c0012 | t0002 | g0112 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04115 | hp2 | a0002 | c0001 | t0007 | g0147 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04184 | hp1 | a0003 | c0002 | t0004 | g0182 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04184 | hp2 | a0001 | c0012 | t0002 | g0133 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04199 | hp1 | a0039 | c0058 | t0017 | g0191 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04199 | hp2 | a0041 | c0053 | t0001 | g0195 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04204 | hp1 | a0022 | c0078 | t0005 | g0063 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04204 | hp2 | a0008 | c0024 | t0001 | g0306 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04228 | hp1 | a0003 | c0002 | t0004 | g0229 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG04228 | hp2 | a0002 | c0062 | t0007 | g0152 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18612 | hp1 | a0003 | c0002 | t0004 | g0280 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18612 | hp2 | a0031 | c0091 | t0001 | g0042 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0035 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18747 | hp2 | a0001 | c0003 | t0003 | g0083 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18906 | hp1 | a0004 | c0004 | t0002 | g0156 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0169 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18942 | hp1 | a0003 | c0002 | t0004 | g0295 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18942 | hp2 | a0001 | c0086 | t0003 | g0031 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18944 | hp1 | a0003 | c0002 | t0001 | g0062 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18944 | hp2 | a0005 | c0028 | t0001 | g0226 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18947 | hp1 | a0001 | c0003 | t0003 | g0110 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0187 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18948 | hp1 | a0003 | c0002 | t0001 | g0096 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18948 | hp2 | a0005 | c0005 | t0008 | g0078 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18950 | hp1 | a0001 | c0026 | t0003 | g0247 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18950 | hp2 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18951 | hp1 | a0005 | c0065 | t0005 | g0179 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18951 | hp2 | a0001 | c0003 | t0003 | g0053 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18952 | hp2 | a0001 | c0003 | t0003 | g0300 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18962 | hp1 | a0001 | c0003 | t0003 | g0259 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18962 | hp2 | a0002 | c0076 | t0001 | g0303 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18963 | hp1 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18963 | hp2 | a0005 | c0096 | t0005 | g0199 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18964 | hp1 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18964 | hp2 | a0050 | c0043 | t0004 | g0060 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18966 | hp1 | a0003 | c0064 | t0005 | g0198 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18966 | hp2 | a0003 | c0002 | t0001 | g0095 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18967 | hp1 | a0001 | c0026 | t0003 | g0246 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18967 | hp2 | a0003 | c0002 | t0001 | g0103 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18969 | hp1 | a0037 | c0060 | t0032 | g0125 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18969 | hp2 | a0056 | c0100 | t0001 | g0237 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18970 | hp1 | a0042 | c0075 | t0001 | g0085 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18970 | hp2 | a0001 | c0019 | t0003 | g0294 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18971 | hp1 | a0001 | c0010 | t0001 | g0034 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0278 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18975 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18977 | hp1 | a0001 | c0003 | t0003 | g0258 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18977 | hp2 | a0001 | c0010 | t0001 | g0255 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18980 | hp1 | a0032 | c0071 | t0003 | g0006 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18980 | hp2 | a0003 | c0018 | t0001 | g0307 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18981 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18981 | hp2 | a0044 | c0050 | t0001 | g0102 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0279 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18982 | hp2 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18983 | hp1 | a0001 | c0019 | t0003 | g0315 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18983 | hp2 | a0001 | c0019 | t0003 | g0200 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18984 | hp1 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18984 | hp2 | a0001 | c0003 | t0003 | g0059 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18986 | hp2 | a0036 | c0061 | t0003 | g0189 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18990 | hp1 | a0001 | c0068 | t0008 | g0070 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA18990 | hp2 | a0003 | c0002 | t0001 | g0039 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19002 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19002 | hp2 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19005 | hp1 | a0003 | c0002 | t0001 | g0056 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19007 | hp1 | a0001 | c0003 | t0003 | g0044 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19007 | hp2 | a0003 | c0002 | t0004 | g0122 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0285 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19009 | hp2 | a0002 | c0055 | t0005 | g0283 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0314 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19010 | hp2 | a0002 | c0072 | t0001 | g0080 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19011 | hp1 | a0005 | c0005 | t0008 | g0087 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19011 | hp2 | a0003 | c0002 | t0001 | g0104 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0291 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19012 | hp2 | a0002 | c0057 | t0003 | g0284 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19030 | hp1 | a0016 | c0030 | t0007 | g0239 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19030 | hp2 | a0004 | c0004 | t0002 | g0221 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19043 | hp1 | a0007 | c0008 | t0004 | g0317 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19043 | hp2 | a0001 | c0007 | t0015 | g0275 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19060 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19060 | hp2 | a0001 | c0025 | t0003 | g0065 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0076 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19066 | hp2 | a0005 | c0005 | t0005 | g0202 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19080 | hp1 | a0001 | c0085 | t0001 | g0073 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19080 | hp2 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19082 | hp1 | a0002 | c0016 | t0001 | g0052 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19082 | hp2 | a0002 | c0052 | t0001 | g0045 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19083 | hp1 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19083 | hp2 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19085 | hp1 | a0003 | c0002 | t0001 | g0049 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19085 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0287 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19088 | hp2 | a0002 | c0001 | t0001 | g0321 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19240 | hp1 | a0018 | c0039 | t0011 | g0270 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA19240 | hp2 | a0004 | c0004 | t0002 | g0138 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20129 | hp1 | a0014 | c0022 | t0036 | g0318 | AFR | ASW | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0131 | AFR | ASW | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20805 | hp1 | a0004 | c0004 | t0002 | g0214 | EUR | TSI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20805 | hp2 | a0006 | c0006 | t0001 | g0201 | EUR | TSI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20905 | hp1 | a0011 | c0015 | t0001 | g0166 | SAS | GIH | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20905 | hp2 | a0003 | c0002 | t0004 | g0115 | SAS | GIH | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01123 | hp1 | a0001 | c0012 | t0002 | g0137 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG01123 | hp2 | a0006 | c0006 | t0001 | g0009 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02109 | hp1 | a0001 | c0007 | t0016 | g0234 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02109 | hp2 | a0049 | c0098 | t0002 | g0267 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02486 | hp1 | a0018 | c0106 | t0010 | g0328 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02486 | hp2 | a0004 | c0004 | t0002 | g0217 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02559 | hp1 | a0006 | c0020 | t0002 | g0238 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG02559 | hp2 | a0013 | c0027 | t0001 | g0026 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03471 | hp1 | a0001 | c0009 | t0037 | g0319 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG03471 | hp2 | a0004 | c0004 | t0029 | g0220 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG06807 | hp1 | a0001 | c0093 | t0001 | g0145 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
HG06807 | hp2 | a0001 | c0009 | t0024 | g0248 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20300 | hp1 | a0019 | c0105 | t0001 | g0249 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA20300 | hp2 | a0003 | c0002 | t0001 | g0097 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA21309 | hp1 | a0010 | c0031 | t0004 | g0018 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
NA21309 | hp2 | a0057 | c0104 | t0010 | g0160 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0002 | g0007 | REF | REF | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
homoSapiens_grch38 | hp1 | a0051 | c0042 | t0003 | g0011 | REF | REF | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81399839
|
G | GGGCCCGC others(5): Show |
1 | a0057 | 1 | NA21309.hp2 | disruptive_inframe_insertion | MODERATE | c.101_112dupGGCCCGCC others(4): Show |
p.Ala37_Gln38insArgP others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 498/10726 | 113/7827 | 38/2608 | INFO_REALIGN_3_PRIME | chr17 | 81399839 | |
chr17:81441921
|
A | C | 1 | a0056 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.572A>C | p.His191Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 957/10726 | 572/7827 | 191/2608 | chr17 | 81441921 | ||
chr17:81441922
|
C | A | 1 | a0056 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.573C>A | p.His191Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 958/10726 | 573/7827 | 191/2608 | chr17 | 81441922 | ||
chr17:81442163
|
G | A | 8 | a0004a0015a0018others(5): Show | 45 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
missense_variant | MODERATE | c.814G>A | p.Ala272Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1199/10726 | 814/7827 | 272/2608 | chr17 | 81442163 | ||
chr17:81442283
|
A | G | 56 | a0001a0002a0003others(53): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
missense_variant | MODERATE | c.934A>G | p.Thr312Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1319/10726 | 934/7827 | 312/2608 | chr17 | 81442283 | ||
chr17:81442301
|
G | A | 1 | a0050 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.952G>A | p.Gly318Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1337/10726 | 952/7827 | 318/2608 | chr17 | 81442301 | ||
chr17:81442391
|
G | A | 2 | a0014a0049 | 4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.1042G>A | p.Ala348Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1427/10726 | 1042/7827 | 348/2608 | chr17 | 81442391 | ||
chr17:81442400
|
G | A | 1 | a0055 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.1051G>A | p.Ala351Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1436/10726 | 1051/7827 | 351/2608 | chr17 | 81442400 | ||
chr17:81442403
|
G | A | 3 | a0046a0047a0048 | 3 | HG01884.hp2 HG02717.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.1054G>A | p.Gly352Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1439/10726 | 1054/7827 | 352/2608 | chr17 | 81442403 | ||
chr17:81442580
|
G | A | 1 | a0007 | 7 | HG01243.hp2 HG01891.hp1 HG02809.hp2 others(4): Show |
missense_variant | MODERATE | c.1231G>A | p.Ala411Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1616/10726 | 1231/7827 | 411/2608 | chr17 | 81442580 | ||
chr17:81442616
|
C | T | 1 | a0045 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1267C>T | p.Arg423Trp | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1652/10726 | 1267/7827 | 423/2608 | chr17 | 81442616 | ||
chr17:81442617
|
G | A | 1 | a0020 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1268G>A | p.Arg423Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1653/10726 | 1268/7827 | 423/2608 | chr17 | 81442617 | ||
chr17:81443549
|
G | A | 1 | a0044 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.2200G>A | p.Ala734Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2585/10726 | 2200/7827 | 734/2608 | chr17 | 81443549 | ||
chr17:81443902
|
G | T | 1 | a0021 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2309G>T | p.Arg770Leu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/28 | 2694/10726 | 2309/7827 | 770/2608 | chr17 | 81443902 | ||
chr17:81444486
|
C | A | 2 | a0009a0013 | 8 | HG01192.hp2 HG01928.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.2430C>A | p.Asp810Glu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 7/28 | 2815/10726 | 2430/7827 | 810/2608 | chr17 | 81444486 | ||
chr17:81444552
|
G | T | 1 | a0022 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2496G>T | p.Met832Ile | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 7/28 | 2881/10726 | 2496/7827 | 832/2608 | chr17 | 81444552 | ||
chr17:81444796
|
C | T | 1 | a0043 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2641C>T | p.Pro881Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/28 | 3026/10726 | 2641/7827 | 881/2608 | chr17 | 81444796 | ||
chr17:81445060
|
G | T | 1 | a0042 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.2717G>T | p.Gly906Val | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 9/28 | 3102/10726 | 2717/7827 | 906/2608 | chr17 | 81445060 | ||
chr17:81445439
|
C | A | 2 | a0006a0049 | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
missense_variant | MODERATE | c.2921C>A | p.Thr974Asn | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3306/10726 | 2921/7827 | 974/2608 | chr17 | 81445439 | ||
chr17:81445525
|
G | A | 1 | a0041 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.3007G>A | p.Ala1003Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3392/10726 | 3007/7827 | 1003/2608 | chr17 | 81445525 | ||
chr17:81447057
|
G | A | 1 | a0057 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3185G>A | p.Arg1062His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3570/10726 | 3185/7827 | 1062/2608 | chr17 | 81447057 | ||
chr17:81447281
|
A | G | 35 | a0001a0003a0004others(32): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
missense_variant | MODERATE | c.3409A>G | p.Thr1137Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3794/10726 | 3409/7827 | 1137/2608 | chr17 | 81447281 | ||
chr17:81447417
|
G | A | 1 | a0011 | 3 | HG02735.hp1 HG03669.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.3545G>A | p.Arg1182Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3930/10726 | 3545/7827 | 1182/2608 | chr17 | 81447417 | ||
chr17:81447608
|
G | A | 2 | a0006a0049 | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
missense_variant | MODERATE | c.3736G>A | p.Gly1246Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4121/10726 | 3736/7827 | 1246/2608 | chr17 | 81447608 | ||
chr17:81447639
|
C | T | 1 | a0035 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.3767C>T | p.Ala1256Val | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4152/10726 | 3767/7827 | 1256/2608 | chr17 | 81447639 | ||
chr17:81447737
|
C | A | 1 | a0040 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.3865C>A | p.Pro1289Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4250/10726 | 3865/7827 | 1289/2608 | chr17 | 81447737 | ||
chr17:81451999
|
G | A | 11 | a0003a0004a0018others(8): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
missense_variant | MODERATE | c.4208G>A | p.Arg1403Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/28 | 4593/10726 | 4208/7827 | 1403/2608 | chr17 | 81451999 | ||
chr17:81452835
|
G | A | 1 | a0048 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.4429G>A | p.Asp1477Asn | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/28 | 4814/10726 | 4429/7827 | 1477/2608 | chr17 | 81452835 | ||
chr17:81455361
|
G | A | 2 | a0005a0028 | 15 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(12): Show |
missense_variant | MODERATE | c.4540G>A | p.Val1514Ile | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/28 | 4925/10726 | 4540/7827 | 1514/2608 | chr17 | 81455361 | ||
chr17:81455365
|
A | G | 1 | a0029 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.4544A>G | p.Tyr1515Cys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/28 | 4929/10726 | 4544/7827 | 1515/2608 | chr17 | 81455365 | ||
chr17:81455368
|
C | T | 1 | a0034 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.4547C>T | p.Ala1516Val | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/28 | 4932/10726 | 4547/7827 | 1516/2608 | chr17 | 81455368 | ||
chr17:81456347
|
CGTGGCCC others(5): Show |
C | 1 | a0053 | 1 | HG02258.hp1 | disruptive_inframe_deletion | MODERATE | c.4629_4640delCAGGGT others(6): Show |
p.His1543_Ala1546del | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/28 | 5014/10726 | 4629/7827 | 1543/2608 | INFO_REALIGN_3_PRIME | chr17 | 81456347 | |
chr17:81456525
|
G | A | 1 | a0056 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.4798G>A | p.Gly1600Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/28 | 5183/10726 | 4798/7827 | 1600/2608 | chr17 | 81456525 | ||
chr17:81457490
|
A | G | 34 | a0001a0003a0004others(31): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
missense_variant | MODERATE | c.4939A>G | p.Thr1647Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5324/10726 | 4939/7827 | 1647/2608 | chr17 | 81457490 | ||
chr17:81458372
|
G | A | 1 | a0010 | 3 | HG02258.hp2 HG02895.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.5249G>A | p.Arg1750Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5634/10726 | 5249/7827 | 1750/2608 | chr17 | 81458372 | ||
chr17:81458411
|
G | A | 1 | a0037 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.5288G>A | p.Ser1763Asn | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5673/10726 | 5288/7827 | 1763/2608 | chr17 | 81458411 | ||
chr17:81458443
|
A | C | 1 | a0023 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.5320A>C | p.Thr1774Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5705/10726 | 5320/7827 | 1774/2608 | chr17 | 81458443 | ||
chr17:81458645
|
A | G | 2 | a0010a0016 | 5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.5368A>G | p.Thr1790Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 19/28 | 5753/10726 | 5368/7827 | 1790/2608 | chr17 | 81458645 | ||
chr17:81459285
|
A | G | 1 | a0026 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.5753A>G | p.Asn1918Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/28 | 6138/10726 | 5753/7827 | 1918/2608 | chr17 | 81459285 | ||
chr17:81460363
|
G | A | 2 | a0030a0038 | 2 | HG03209.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.5992G>A | p.Val1998Ile | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/28 | 6377/10726 | 5992/7827 | 1998/2608 | chr17 | 81460363 | ||
chr17:81460920
|
A | G | 2 | a0017a0018 | 4 | HG02486.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.6257A>G | p.His2086Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6642/10726 | 6257/7827 | 2086/2608 | chr17 | 81460920 | ||
chr17:81460932
|
G | A | 1 | a0024 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.6269G>A | p.Arg2090His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6654/10726 | 6269/7827 | 2090/2608 | chr17 | 81460932 | ||
chr17:81460935
|
G | A | 2 | a0025a0031 | 2 | HG03579.hp2 NA18612.hp2 |
missense_variant | MODERATE | c.6272G>A | p.Arg2091His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6657/10726 | 6272/7827 | 2091/2608 | chr17 | 81460935 | ||
chr17:81460961
|
G | A | 1 | a0033 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.6298G>A | p.Ala2100Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6683/10726 | 6298/7827 | 2100/2608 | chr17 | 81460961 | ||
chr17:81461093
|
G | A | 1 | a0032 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.6430G>A | p.Val2144Met | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6815/10726 | 6430/7827 | 2144/2608 | chr17 | 81461093 | ||
chr17:81461336
|
G | T | 1 | a0039 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.6673G>T | p.Ala2225Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7058/10726 | 6673/7827 | 2225/2608 | chr17 | 81461336 | ||
chr17:81461793
|
G | A | 1 | a0046 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.7130G>A | p.Arg2377His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7515/10726 | 7130/7827 | 2377/2608 | chr17 | 81461793 | ||
chr17:81462870
|
G | A | 1 | a0052 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.7514G>A | p.Arg2505His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/28 | 7899/10726 | 7514/7827 | 2505/2608 | chr17 | 81462870 | ||
chr17:81463711
|
G | A | 4 | a0012a0028a0040others(1): Show | 6 | HG01106.hp2 HG01346.hp1 HG01975.hp1 others(3): Show |
missense_variant | MODERATE | c.7721G>A | p.Arg2574Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 8106/10726 | 7721/7827 | 2574/2608 | chr17 | 81463711 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81399811
|
C | T | 3 | a0018c0106a0019c0105a0025c0107 | 3 | HG02486.hp1 HG03579.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.72C>T | p.Ala24Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 457/10726 | 72/7827 | 24/2608 | chr17 | 81399811 | ||
chr17:81399895
|
G | A | 1 | a0001c0032 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.156G>A | p.Pro52Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 541/10726 | 156/7827 | 52/2608 | chr17 | 81399895 | ||
chr17:81426873
|
G | A | 1 | a0034c0033 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.252G>A | p.Ser84Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/28 | 637/10726 | 252/7827 | 84/2608 | chr17 | 81426873 | ||
chr17:81426891
|
C | G | 1 | a0001c0103 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.270C>G | p.Pro90Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/28 | 655/10726 | 270/7827 | 90/2608 | chr17 | 81426891 | ||
chr17:81441898
|
C | T | 3 | a0001c0101a0010c0031a0010c0102 | 4 | HG02258.hp2 HG02895.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.549C>T | p.Ser183Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 934/10726 | 549/7827 | 183/2608 | chr17 | 81441898 | ||
chr17:81441994
|
C | T | 1 | a0001c0099 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.645C>T | p.Phe215Phe | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1030/10726 | 645/7827 | 215/2608 | chr17 | 81441994 | ||
chr17:81442264
|
C | T | 2 | a0014c0022a0049c0098 | 4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
synonymous_variant | LOW | c.915C>T | p.Gly305Gly | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1300/10726 | 915/7827 | 305/2608 | chr17 | 81442264 | ||
chr17:81442345
|
G | A | 1 | a0002c0044 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.996G>A | p.Pro332Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1381/10726 | 996/7827 | 332/2608 | chr17 | 81442345 | ||
chr17:81442348
|
C | T | 1 | a0013c0097 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.999C>T | p.Ala333Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1384/10726 | 999/7827 | 333/2608 | chr17 | 81442348 | ||
chr17:81442408
|
A | C | 1 | a0004c0035 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1059A>C | p.Pro353Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1444/10726 | 1059/7827 | 353/2608 | chr17 | 81442408 | ||
chr17:81442408
|
A | G | 50 | a0001c0007a0001c0021a0001c0025others(47): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
synonymous_variant | LOW | c.1059A>G | p.Pro353Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1444/10726 | 1059/7827 | 353/2608 | chr17 | 81442408 | ||
chr17:81442502
|
C | A | 1 | a0017c0023 | 2 | HG02717.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.1153C>A | p.Arg385Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1538/10726 | 1153/7827 | 385/2608 | chr17 | 81442502 | ||
chr17:81442588
|
C | T | 1 | a0002c0081 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1239C>T | p.Ala413Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1624/10726 | 1239/7827 | 413/2608 | chr17 | 81442588 | ||
chr17:81442684
|
G | A | 12 | a0004c0004a0004c0035a0004c0037others(9): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
synonymous_variant | LOW | c.1335G>A | p.Lys445Lys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1720/10726 | 1335/7827 | 445/2608 | chr17 | 81442684 | ||
chr17:81443164
|
C | T | 1 | a0054c0041 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1815C>T | p.Tyr605Tyr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2200/10726 | 1815/7827 | 605/2608 | chr17 | 81443164 | ||
chr17:81443230
|
G | A | 10 | a0001c0025a0001c0026a0001c0085others(7): Show | 54 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(51): Show |
synonymous_variant | LOW | c.1881G>A | p.Pro627Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2266/10726 | 1881/7827 | 627/2608 | chr17 | 81443230 | ||
chr17:81443518
|
C | T | 1 | a0010c0102 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2169C>T | p.Tyr723Tyr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2554/10726 | 2169/7827 | 723/2608 | chr17 | 81443518 | ||
chr17:81444798
|
C | G | 1 | a0002c0076 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.2643C>G | p.Pro881Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/28 | 3028/10726 | 2643/7827 | 881/2608 | chr17 | 81444798 | ||
chr17:81445091
|
G | A | 1 | a0001c0051 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.2748G>A | p.Pro916Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 9/28 | 3133/10726 | 2748/7827 | 916/2608 | chr17 | 81445091 | ||
chr17:81445380
|
T | C | 1 | a0002c0052 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.2862T>C | p.Asp954Asp | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3247/10726 | 2862/7827 | 954/2608 | chr17 | 81445380 | ||
chr17:81445392
|
C | T | 1 | a0002c0074 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.2874C>T | p.Pro958Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3259/10726 | 2874/7827 | 958/2608 | chr17 | 81445392 | ||
chr17:81445440
|
C | T | 1 | a0008c0073 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.2922C>T | p.Thr974Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3307/10726 | 2922/7827 | 974/2608 | chr17 | 81445440 | ||
chr17:81445452
|
G | A | 2 | a0013c0027a0013c0097 | 3 | HG02559.hp2 HG02615.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.2934G>A | p.Pro978Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3319/10726 | 2934/7827 | 978/2608 | chr17 | 81445452 | ||
chr17:81445461
|
C | T | 1 | a0005c0096 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.2943C>T | p.Pro981Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3328/10726 | 2943/7827 | 981/2608 | chr17 | 81445461 | ||
chr17:81445524
|
C | T | 1 | a0002c0072 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.3006C>T | p.Pro1002Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3391/10726 | 3006/7827 | 1002/2608 | chr17 | 81445524 | ||
chr17:81445536
|
C | G | 2 | a0001c0019a0032c0071 | 4 | NA18970.hp2 NA18980.hp1 NA18983.hp1 others(1): Show |
synonymous_variant | LOW | c.3018C>G | p.Pro1006Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3403/10726 | 3018/7827 | 1006/2608 | chr17 | 81445536 | ||
chr17:81445563
|
G | A | 1 | a0056c0100 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.3045G>A | p.Pro1015Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3430/10726 | 3045/7827 | 1015/2608 | chr17 | 81445563 | ||
chr17:81445596
|
C | T | 1 | a0001c0026 | 2 | NA18950.hp1 NA18967.hp1 |
synonymous_variant | LOW | c.3078C>T | p.Pro1026Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3463/10726 | 3078/7827 | 1026/2608 | chr17 | 81445596 | ||
chr17:81447295
|
C | T | 3 | a0002c0063a0019c0105a0057c0104 | 3 | HG02809.hp1 NA20300.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.3423C>T | p.Pro1141Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3808/10726 | 3423/7827 | 1141/2608 | chr17 | 81447295 | ||
chr17:81447769
|
A | G | 1 | a0001c0094 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.3897A>G | p.Ser1299Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4282/10726 | 3897/7827 | 1299/2608 | chr17 | 81447769 | ||
chr17:81447778
|
T | C | 3 | a0006c0006a0006c0020a0049c0098 | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
synonymous_variant | LOW | c.3906T>C | p.His1302His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4291/10726 | 3906/7827 | 1302/2608 | chr17 | 81447778 | ||
chr17:81451726
|
C | T | 1 | a0002c0062 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.4035C>T | p.Ala1345Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/28 | 4420/10726 | 4035/7827 | 1345/2608 | chr17 | 81451726 | ||
chr17:81451744
|
C | T | 25 | a0001c0003a0001c0010a0001c0019others(22): Show | 61 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(58): Show |
synonymous_variant | LOW | c.4053C>T | p.Ala1351Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/28 | 4438/10726 | 4053/7827 | 1351/2608 | chr17 | 81451744 | ||
chr17:81457462
|
A | G | 1 | a0001c0093 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.4911A>G | p.Pro1637Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5296/10726 | 4911/7827 | 1637/2608 | chr17 | 81457462 | ||
chr17:81457492
|
C | T | 1 | a0005c0028 | 2 | HG02083.hp2 NA18944.hp2 |
synonymous_variant | LOW | c.4941C>T | p.Thr1647Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5326/10726 | 4941/7827 | 1647/2608 | chr17 | 81457492 | ||
chr17:81457511
|
C | T | 19 | a0001c0085a0003c0002a0003c0018others(16): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
synonymous_variant | LOW | c.4960C>T | p.Leu1654Leu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5345/10726 | 4960/7827 | 1654/2608 | chr17 | 81457511 | ||
chr17:81457564
|
G | A | 1 | a0004c0037 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.5013G>A | p.Lys1671Lys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5398/10726 | 5013/7827 | 1671/2608 | chr17 | 81457564 | ||
chr17:81458295
|
C | T | 2 | a0001c0019a0032c0071 | 4 | NA18970.hp2 NA18980.hp1 NA18983.hp1 others(1): Show |
synonymous_variant | LOW | c.5172C>T | p.Ala1724Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5557/10726 | 5172/7827 | 1724/2608 | chr17 | 81458295 | ||
chr17:81458959
|
C | T | 1 | a0038c0059 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.5595C>T | p.Ser1865Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/28 | 5980/10726 | 5595/7827 | 1865/2608 | chr17 | 81458959 | ||
chr17:81459154
|
G | T | 1 | a0001c0086 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.5706G>T | p.Leu1902Leu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 21/28 | 6091/10726 | 5706/7827 | 1902/2608 | chr17 | 81459154 | ||
chr17:81460329
|
C | T | 1 | a0001c0069 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.5958C>T | p.Asp1986Asp | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/28 | 6343/10726 | 5958/7827 | 1986/2608 | chr17 | 81460329 | ||
chr17:81460341
|
A | C | 2 | a0010c0031a0010c0102 | 3 | HG02258.hp2 HG02895.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.5970A>C | p.Thr1990Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/28 | 6355/10726 | 5970/7827 | 1990/2608 | chr17 | 81460341 | ||
chr17:81460906
|
G | A | 1 | a0002c0016 | 3 | HG02129.hp2 HG02135.hp1 NA19082.hp1 |
synonymous_variant | LOW | c.6243G>A | p.Thr2081Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6628/10726 | 6243/7827 | 2081/2608 | chr17 | 81460906 | ||
chr17:81461389
|
C | T | 1 | a0001c0093 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.6726C>T | p.Pro2242Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7111/10726 | 6726/7827 | 2242/2608 | chr17 | 81461389 | ||
chr17:81461572
|
G | A | 6 | a0001c0068a0002c0055a0003c0064others(3): Show | 14 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(11): Show |
synonymous_variant | LOW | c.6909G>A | p.Ala2303Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7294/10726 | 6909/7827 | 2303/2608 | chr17 | 81461572 | ||
chr17:81461575
|
C | T | 9 | a0001c0012a0001c0021a0006c0020others(6): Show | 19 | HG00099.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
synonymous_variant | LOW | c.6912C>T | p.Ala2304Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7297/10726 | 6912/7827 | 2304/2608 | chr17 | 81461575 | ||
chr17:81462769
|
G | A | 1 | a0002c0056 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.7413G>A | p.Lys2471Lys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/28 | 7798/10726 | 7413/7827 | 2471/2608 | chr17 | 81462769 | ||
chr17:81462826
|
C | T | 19 | a0001c0003a0001c0019a0001c0025others(16): Show | 50 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
synonymous_variant | LOW | c.7470C>T | p.Ala2490Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/28 | 7855/10726 | 7470/7827 | 2490/2608 | chr17 | 81462826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81399639
|
C | T | 1 | a0017c0023t0038 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 101 | chr17 | 81399639 | |||||
chr17:81399674
|
A | G | 2 | a0001c0009t0037a0014c0022t0036 | 2 | HG03471.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-66A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 66 | chr17 | 81399674 | |||||
chr17:81463822
|
C | A | 1 | a0039c0058t0017 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 5 | chr17 | 81463822 | |||||
chr17:81463852
|
G | A | 3 | a0001c0007t0009a0001c0010t0009a0001c0094t0009 | 4 | HG02622.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*35G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 35 | chr17 | 81463852 | |||||
chr17:81463865
|
G | A | 1 | a0002c0001t0018 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 48 | chr17 | 81463865 | |||||
chr17:81464292
|
G | A | 6 | a0001c0009t0006a0002c0001t0006a0002c0063t0020others(3): Show | 9 | HG01192.hp2 HG01261.hp1 HG01515.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 475 | chr17 | 81464292 | |||||
chr17:81464405
|
C | T | 1 | a0003c0002t0013 | 3 | HG02257.hp2 HG02886.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*588C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 588 | chr17 | 81464405 | |||||
chr17:81464733
|
A | G | 1 | a0003c0002t0035 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*916A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 916 | chr17 | 81464733 | |||||
chr17:81464817
|
G | A | 31 | a0001c0007t0002a0001c0012t0002a0001c0021t0002others(28): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1000G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1000 | chr17 | 81464817 | |||||
chr17:81464817
|
G | C | 1 | a0004c0011t0023 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1000G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1000 | chr17 | 81464817 | |||||
chr17:81464977
|
G | A | 7 | a0001c0009t0006a0001c0009t0024a0001c0009t0025others(4): Show | 10 | HG01192.hp2 HG01261.hp1 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1160G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1160 | chr17 | 81464977 | |||||
chr17:81465013
|
C | T | 1 | a0004c0004t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1196C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1196 | chr17 | 81465013 | |||||
chr17:81465074
|
C | T | 1 | a0005c0066t0034 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1257C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1257 | chr17 | 81465074 | |||||
chr17:81465176
|
T | C | 60 | a0001c0003t0010a0001c0007t0002a0001c0007t0015others(57): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1359T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1359 | chr17 | 81465176 | |||||
chr17:81465237
|
A | C | 3 | a0001c0007t0009a0001c0010t0009a0001c0094t0009 | 4 | HG02622.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1420A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1420 | chr17 | 81465237 | |||||
chr17:81465325
|
C | T | 15 | a0001c0007t0009a0001c0009t0025a0001c0010t0009others(12): Show | 22 | HG00438.hp2 HG01069.hp2 HG01261.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1508C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1508 | chr17 | 81465325 | |||||
chr17:81465370
|
C | T | 2 | a0001c0068t0008a0005c0005t0008 | 6 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1553C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1553 | chr17 | 81465370 | |||||
chr17:81465375
|
C | T | 19 | a0001c0009t0004a0001c0009t0030a0001c0009t0037others(16): Show | 36 | HG00544.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1558C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1558 | chr17 | 81465375 | |||||
chr17:81465403
|
G | A | 55 | a0001c0007t0002a0001c0007t0009a0001c0009t0004others(52): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1586G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1586 | chr17 | 81465403 | |||||
chr17:81465569
|
G | T | 2 | a0001c0009t0030a0001c0009t0037 | 2 | HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1752G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1752 | chr17 | 81465569 | |||||
chr17:81465645
|
T | C | 117 | a0001c0007t0002a0001c0007t0009a0001c0009t0004others(114): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*1828T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1828 | chr17 | 81465645 | |||||
chr17:81465671
|
C | A | 1 | a0002c0001t0031 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1854C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1854 | chr17 | 81465671 | |||||
chr17:81465810
|
G | A | 1 | a0008c0029t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1993G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1993 | chr17 | 81465810 | |||||
chr17:81466037
|
C | A | 1 | a0001c0103t0026 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2220C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2220 | chr17 | 81466037 | |||||
chr17:81466055
|
C | T | 1 | a0001c0007t0033 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2238C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2238 | chr17 | 81466055 | |||||
chr17:81466080
|
C | T | 121 | a0001c0007t0002a0001c0007t0009a0001c0007t0015others(118): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*2263C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2263 | chr17 | 81466080 | |||||
chr17:81466103
|
G | A | 1 | a0054c0041t0019 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2286G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2286 | chr17 | 81466103 | |||||
chr17:81466134
|
G | A | 2 | a0039c0058t0017a0046c0047t0027 | 2 | HG03516.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2317G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2317 | chr17 | 81466134 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81395658
|
A | AT | 202 | a0001c0003t0003g0184a0001c0003t0003g0186a0001c0003t0003g0208others(199): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-207+33dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81395658 | |||||
chr17:81395807
|
C | CT | 91 | a0001c0003t0003g0184a0001c0003t0003g0186a0001c0003t0003g0208others(88): Show | 91 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-207+182dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81395807 | |||||
chr17:81395807
|
C | CTT | 179 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(176): Show | 182 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-207+181_-207+182d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81395807 | |||||
chr17:81395996
|
C | G | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-207+361C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81395996 | ||||||
chr17:81396027
|
A | C | 304 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-207+392A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396027 | ||||||
chr17:81396110
|
C | G | 1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-207+475C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396110 | ||||||
chr17:81396200
|
T | G | 1 | a0002c0056t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-207+565T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396200 | ||||||
chr17:81396293
|
T | C | 1 | a0002c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-207+658T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396293 | ||||||
chr17:81396457
|
C | G | 32 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-207+822C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396457 | ||||||
chr17:81396532
|
G | A | 1 | a0007c0008t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-207+897G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396532 | ||||||
chr17:81396615
|
C | T | 1 | a0004c0004t0002g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-207+980C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396615 | ||||||
chr17:81396707
|
A | G | 1 | a0002c0001t0001g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-207+1072A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396707 | ||||||
chr17:81396722
|
C | G | 1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-207+1087C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396722 | ||||||
chr17:81396854
|
C | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-207+1219C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396854 | ||||||
chr17:81396861
|
C | G | 1 | a0018c0106t0010g0328 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-207+1226C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396861 | ||||||
chr17:81396868
|
C | T | 1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-207+1233C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396868 | ||||||
chr17:81396894
|
C | T | 6 | a0002c0001t0001g0324a0002c0001t0001g0326a0002c0001t0001g0327others(3): Show | 6 | HG01074.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-207+1259C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396894 | ||||||
chr17:81396900
|
C | G | 319 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(316): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-207+1265C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396900 | ||||||
chr17:81396952
|
C | A | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-207+1317C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396952 | ||||||
chr17:81397039
|
G | A | 2 | a0001c0026t0003g0246a0001c0026t0003g0247 | 2 | NA18950.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-207+1404G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397039 | ||||||
chr17:81397090
|
C | T | 1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-207+1455C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397090 | ||||||
chr17:81397275
|
C | T | 1 | a0002c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-207+1640C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397275 | ||||||
chr17:81397296
|
G | A | 1 | a0002c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-207+1661G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397296 | ||||||
chr17:81397393
|
G | A | 8 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0069t0007g0253others(5): Show | 8 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+1758G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397393 | ||||||
chr17:81397395
|
G | A | 8 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0069t0007g0253others(5): Show | 8 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+1760G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397395 | ||||||
chr17:81397395
|
G | GA | 28 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-207+1777dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81397395 | |||||
chr17:81397407
|
A | C | 1 | a0002c0001t0001g0321 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-207+1772A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397407 | ||||||
chr17:81397410
|
A | AC | 19 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0010t0001g0255others(16): Show | 19 | HG00609.hp2 HG01074.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-207+1775_-207+177 others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397410 | ||||||
chr17:81397410
|
A | C | 254 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(251): Show | 257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.-207+1775A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397410 | ||||||
chr17:81397414
|
A | C | 4 | a0004c0004t0002g0167a0004c0004t0002g0240a0004c0004t0002g0241others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+1779A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397414 | ||||||
chr17:81397430
|
C | T | 5 | a0001c0086t0003g0031a0002c0001t0001g0030a0002c0044t0001g0164others(2): Show | 5 | HG00609.hp2 HG03491.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-207+1795C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397430 | ||||||
chr17:81397525
|
T | A | 1 | a0003c0002t0001g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-207+1890T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397525 | ||||||
chr17:81397537
|
A | T | 1 | a0037c0060t0032g0125 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-207+1902A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397537 | ||||||
chr17:81397623
|
G | A | 31 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-206-1911G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397623 | ||||||
chr17:81397638
|
C | T | 1 | a0002c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-206-1896C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397638 | ||||||
chr17:81397912
|
G | A | 1 | a0001c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-206-1622G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397912 | ||||||
chr17:81398035
|
A | T | 1 | a0004c0004t0002g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-206-1499A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398035 | ||||||
chr17:81398208
|
T | G | 1 | a0002c0001t0018g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-206-1326T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398208 | ||||||
chr17:81398486
|
GCCGCCCG others(3): Show |
G | 11 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0009t0037g0319others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-206-1046_-206-103 others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398486 | |||||
chr17:81398525
|
C | T | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-206-1009C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398525 | ||||||
chr17:81398606
|
AC | A | 171 | a0001c0003t0003g0184a0001c0003t0003g0186a0001c0003t0003g0208others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-206-920delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398606 | |||||
chr17:81398613
|
C | A | 6 | a0002c0001t0001g0169a0003c0002t0004g0170a0003c0002t0004g0171others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-921C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398613 | ||||||
chr17:81398613
|
C | G | 3 | a0003c0002t0001g0124a0003c0002t0004g0122a0003c0002t0004g0123 | 3 | HG00423.hp2 HG00544.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-206-921C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398613 | ||||||
chr17:81398614
|
CA | C | 3 | a0007c0008t0001g0257a0007c0008t0004g0317a0016c0030t0007g0239 | 3 | HG02965.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-206-919delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398614 | ||||||
chr17:81398689
|
C | T | 30 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(27): Show | 30 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-206-845C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398689 | ||||||
chr17:81398772
|
CGGGCCTC others(2): Show |
C | 172 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(169): Show | 175 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-206-757_-206-749d others(11): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398772 | |||||
chr17:81398819
|
C | G | 1 | a0001c0010t0004g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-206-715C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398819 | ||||||
chr17:81398825
|
A | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-206-709A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398825 | ||||||
chr17:81398933
|
T | TA | 16 | a0001c0007t0016g0161a0001c0009t0030g0263a0001c0021t0002g0262others(13): Show | 17 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-206-587dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398933 | |||||
chr17:81398974
|
C | G | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-206-560C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398974 | ||||||
chr17:81399011
|
G | T | 1 | a0002c0016t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-206-523G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399011 | ||||||
chr17:81399110
|
G | A | 3 | a0004c0004t0002g0167a0004c0004t0002g0240a0004c0004t0002g0241 | 3 | HG00642.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-206-424G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399110 | ||||||
chr17:81399128
|
A | AGT | 25 | a0001c0007t0009g0260a0001c0007t0016g0161a0001c0009t0030g0263others(22): Show | 25 | HG00609.hp2 HG00741.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-206-382_-206-381d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
A | AGTGT | 146 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-206-384_-206-381d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
A | AGTGTGT | 25 | a0001c0003t0003g0230a0001c0003t0003g0231a0001c0003t0003g0233others(22): Show | 25 | HG00423.hp2 HG00639.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-206-386_-206-381d others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
A | AGTGTGTG others(1): Show |
10 | a0004c0004t0002g0003a0004c0004t0002g0269a0004c0004t0002g0271others(7): Show | 11 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-206-388_-206-381d others(10): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
A | AGTGTGTG others(3): Show |
1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-206-390_-206-381d others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
A | AGTGTGTG others(5): Show |
2 | a0002c0001t0001g0276a0017c0023t0015g0277 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-206-392_-206-381d others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
AGTGT | A | 5 | a0003c0002t0004g0205a0005c0005t0012g0204a0005c0005t0012g0206others(2): Show | 5 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-206-384_-206-381d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399128
|
AGTGTGT | A | 42 | a0001c0003t0003g0184a0001c0003t0003g0186a0001c0003t0003g0259others(39): Show | 42 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.-206-386_-206-381d others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | |||||
chr17:81399152
|
T | C | 2 | a0001c0009t0024g0248a0002c0001t0002g0132 | 2 | HG03017.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-206-382T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399152 | ||||||
chr17:81399152
|
T | TGC | 41 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0009t0025g0252others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-206-380_-206-379d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399152 | |||||
chr17:81399220
|
C | A | 1 | a0002c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-206-314C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399220 | ||||||
chr17:81399241
|
A | G | 1 | a0002c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-206-293A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399241 | ||||||
chr17:81399244
|
C | T | 1 | a0005c0066t0034g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-206-290C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399244 | ||||||
chr17:81399289
|
C | T | 2 | a0007c0008t0001g0257a0007c0008t0004g0317 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-206-245C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399289 | ||||||
chr17:81399297
|
C | A | 1 | a0002c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-206-237C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399297 | ||||||
chr17:81399315
|
C | T | 1 | a0001c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-206-219C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399315 | ||||||
chr17:81399342
|
C | A | 40 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(37): Show | 40 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.-206-192C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399342 | ||||||
chr17:81399371
|
G | A | 1 | a0001c0003t0003g0044 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-206-163G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399371 | ||||||
chr17:81399403
|
C | A | 222 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(219): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-206-131C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399403 | ||||||
chr17:81399441
|
G | A | 1 | a0001c0099t0003g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-206-93G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399441 | ||||||
chr17:81399985
|
C | T | 1 | a0002c0001t0001g0203 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.178+68C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81399985 | ||||||
chr17:81399991
|
C | T | 7 | a0002c0001t0001g0131a0002c0062t0007g0152a0006c0006t0001g0150others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+74C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81399991 | ||||||
chr17:81400083
|
A | G | 11 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0009t0037g0319others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+166A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400083 | ||||||
chr17:81400162
|
G | A | 171 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(168): Show | 174 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.178+245G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400162 | ||||||
chr17:81400181
|
C | G | 1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178+264C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400181 | ||||||
chr17:81400218
|
C | A | 1 | a0001c0012t0002g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.178+301C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400218 | ||||||
chr17:81400385
|
C | A | 2 | a0002c0001t0001g0276a0017c0023t0015g0277 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+468C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400385 | ||||||
chr17:81400407
|
G | A | 5 | a0001c0094t0009g0016a0010c0031t0004g0015a0010c0031t0004g0018others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+490G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400407 | ||||||
chr17:81400412
|
A | G | 3 | a0002c0001t0001g0035a0002c0001t0001g0036a0002c0001t0001g0037 | 3 | HG00438.hp1 NA18747.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.178+495A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400412 | ||||||
chr17:81400444
|
T | TA | 19 | a0001c0003t0003g0208a0001c0003t0003g0230a0001c0003t0003g0231others(16): Show | 19 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+530dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81400444 | |||||
chr17:81400479
|
C | T | 1 | a0004c0011t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.178+562C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400479 | ||||||
chr17:81400541
|
G | A | 11 | a0001c0003t0003g0258a0001c0003t0003g0286a0001c0003t0003g0289others(8): Show | 11 | HG02083.hp1 NA18963.hp1 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+624G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400541 | ||||||
chr17:81400566
|
G | A | 2 | a0004c0004t0002g0214a0004c0004t0002g0217 | 2 | HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.178+649G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400566 | ||||||
chr17:81400570
|
A | T | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+653A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400570 | ||||||
chr17:81400581
|
G | A | 1 | a0002c0016t0001g0052 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178+664G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400581 | ||||||
chr17:81400589
|
G | A | 1 | a0006c0006t0001g0009 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.178+672G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400589 | ||||||
chr17:81400594
|
G | A | 3 | a0001c0003t0003g0053a0002c0001t0001g0055a0002c0074t0001g0054 | 3 | HG00423.hp1 NA18951.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.178+677G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400594 | ||||||
chr17:81400729
|
C | T | 1 | a0048c0045t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+812C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400729 | ||||||
chr17:81401308
|
G | C | 2 | a0003c0002t0001g0056a0003c0002t0001g0057 | 2 | HG02027.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.178+1391G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401308 | ||||||
chr17:81401337
|
T | C | 1 | a0002c0001t0002g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.178+1420T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401337 | ||||||
chr17:81401391
|
C | T | 1 | a0004c0004t0002g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.178+1474C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401391 | ||||||
chr17:81401515
|
C | T | 32 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.178+1598C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401515 | ||||||
chr17:81401560
|
G | A | 172 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(169): Show | 175 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.178+1643G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401560 | ||||||
chr17:81401724
|
A | G | 1 | a0001c0010t0001g0034 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.178+1807A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401724 | ||||||
chr17:81401741
|
T | G | 1 | a0001c0009t0006g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.178+1824T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401741 | ||||||
chr17:81401746
|
C | A | 1 | a0001c0012t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.178+1829C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401746 | ||||||
chr17:81401825
|
A | ACT | 123 | a0001c0003t0003g0184a0001c0003t0003g0186a0001c0003t0003g0208others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.178+1912_178+1913d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81401825 | |||||
chr17:81401887
|
C | T | 33 | a0001c0007t0016g0161a0001c0007t0033g0135a0001c0009t0006g0134others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.178+1970C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401887 | ||||||
chr17:81402131
|
C | T | 2 | a0005c0005t0005g0202a0017c0023t0038g0027 | 2 | HG02976.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.178+2214C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402131 | ||||||
chr17:81402198
|
C | A | 31 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+2281C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402198 | ||||||
chr17:81402226
|
C | T | 1 | a0001c0003t0003g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.178+2309C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402226 | ||||||
chr17:81402300
|
G | A | 1 | a0001c0003t0003g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178+2383G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402300 | ||||||
chr17:81402322
|
G | C | 1 | a0002c0001t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.178+2405G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402322 | ||||||
chr17:81402483
|
C | T | 1 | a0001c0012t0002g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.178+2566C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402483 | ||||||
chr17:81402568
|
G | C | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+2651G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402568 | ||||||
chr17:81402623
|
G | A | 2 | a0002c0001t0001g0285a0002c0001t0001g0291 | 2 | NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.178+2706G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402623 | ||||||
chr17:81402787
|
C | T | 1 | a0011c0015t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.178+2870C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402787 | ||||||
chr17:81402820
|
G | A | 11 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0009t0037g0319others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+2903G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402820 | ||||||
chr17:81402902
|
G | C | 1 | a0002c0001t0001g0279 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.178+2985G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402902 | ||||||
chr17:81403072
|
A | C | 8 | a0001c0021t0002g0114a0002c0001t0001g0004a0003c0002t0004g0310others(5): Show | 9 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.178+3155A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403072 | ||||||
chr17:81403148
|
G | A | 1 | a0002c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.178+3231G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403148 | ||||||
chr17:81403156
|
G | A | 1 | a0008c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178+3239G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403156 | ||||||
chr17:81403196
|
C | G | 2 | a0002c0001t0001g0326a0002c0001t0001g0327 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.178+3279C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403196 | ||||||
chr17:81403196
|
C | T | 1 | a0002c0001t0001g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178+3279C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403196 | ||||||
chr17:81403197
|
G | A | 3 | a0001c0009t0030g0263a0001c0021t0002g0262a0046c0047t0027g0264 | 3 | HG02055.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178+3280G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403197 | ||||||
chr17:81403219
|
G | C | 1 | a0002c0001t0001g0176 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.178+3302G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403219 | ||||||
chr17:81403246
|
C | T | 31 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+3329C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403246 | ||||||
chr17:81403401
|
A | T | 174 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(171): Show | 177 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.178+3484A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403401 | ||||||
chr17:81403456
|
A | G | 31 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+3539A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403456 | ||||||
chr17:81403481
|
CA | C | 253 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.178+3577delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81403481 | |||||
chr17:81403481
|
CAA | C | 40 | a0001c0003t0003g0208a0001c0003t0003g0230a0001c0003t0003g0231others(37): Show | 40 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.178+3576_178+3577d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81403481 | |||||
chr17:81403501
|
G | A | 1 | a0002c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.178+3584G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403501 | ||||||
chr17:81403546
|
A | G | 1 | a0003c0002t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.178+3629A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403546 | ||||||
chr17:81403671
|
C | T | 2 | a0005c0005t0012g0206a0005c0005t0012g0207 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.178+3754C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403671 | ||||||
chr17:81403736
|
C | T | 1 | a0003c0002t0004g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.178+3819C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403736 | ||||||
chr17:81403743
|
C | T | 1 | a0040c0054t0001g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.178+3826C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403743 | ||||||
chr17:81403744
|
G | A | 1 | a0003c0002t0001g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.178+3827G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403744 | ||||||
chr17:81403786
|
C | G | 91 | a0001c0003t0003g0053a0001c0003t0003g0059a0001c0003t0003g0067others(88): Show | 92 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.178+3869C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403786 | ||||||
chr17:81403786
|
C | T | 46 | a0001c0003t0003g0184a0001c0003t0003g0186a0001c0003t0003g0259others(43): Show | 46 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.178+3869C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403786 | ||||||
chr17:81403947
|
C | T | 1 | a0001c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.178+4030C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403947 | ||||||
chr17:81403967
|
A | G | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.178+4050A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403967 | ||||||
chr17:81404038
|
C | T | 4 | a0002c0001t0001g0131a0006c0006t0002g0153a0006c0006t0002g0154others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+4121C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404038 | ||||||
chr17:81404410
|
T | C | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+4493T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404410 | ||||||
chr17:81404424
|
C | T | 31 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+4507C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404424 | ||||||
chr17:81404751
|
C | G | 174 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(171): Show | 177 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.178+4834C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404751 | ||||||
chr17:81404792
|
C | T | 1 | a0001c0003t0003g0044 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.178+4875C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404792 | ||||||
chr17:81404793
|
G | A | 31 | a0001c0007t0033g0135a0001c0009t0006g0134a0001c0012t0002g0133others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+4876G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404793 | ||||||
chr17:81405065
|
T | C | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.178+5148T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405065 | ||||||
chr17:81405104
|
G | A | 1 | a0004c0004t0002g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.178+5187G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405104 | ||||||
chr17:81405380
|
A | T | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+5463A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405380 | ||||||
chr17:81405589
|
C | T | 2 | a0003c0002t0004g0205a0023c0084t0003g0129 | 2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.178+5672C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405589 | ||||||
chr17:81405739
|
C | G | 1 | a0002c0001t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.178+5822C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405739 | ||||||
chr17:81405944
|
T | C | 1 | a0012c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178+6027T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405944 | ||||||
chr17:81405955
|
C | G | 2 | a0007c0008t0001g0257a0007c0008t0004g0317 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+6038C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405955 | ||||||
chr17:81406149
|
C | G | 1 | a0006c0006t0001g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.178+6232C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406149 | ||||||
chr17:81406219
|
G | A | 1 | a0003c0002t0001g0062 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.178+6302G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406219 | ||||||
chr17:81406229
|
GCTCCTGG others(24): Show |
G | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178+6317_178+6347d others(33): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81406229 | |||||
chr17:81406340
|
G | A | 3 | a0003c0002t0013g0024a0013c0027t0001g0025a0013c0027t0001g0026 | 3 | HG02559.hp2 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.178+6423G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406340 | ||||||
chr17:81406375
|
G | A | 2 | a0004c0004t0002g0214a0004c0004t0002g0217 | 2 | HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.178+6458G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406375 | ||||||
chr17:81406453
|
G | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+6536G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406453 | ||||||
chr17:81406490
|
C | T | 3 | a0001c0007t0016g0161a0001c0103t0026g0245a0047c0046t0004g0273 | 3 | HG02615.hp1 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.178+6573C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406490 | ||||||
chr17:81406620
|
C | G | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+6703C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406620 | ||||||
chr17:81406633
|
G | A | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+6716G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406633 | ||||||
chr17:81406703
|
G | C | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+6786G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406703 | ||||||
chr17:81406747
|
T | C | 183 | a0001c0003t0003g0046a0001c0003t0003g0053a0001c0003t0003g0059others(180): Show | 186 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.178+6830T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406747 | ||||||
chr17:81406750
|
G | A | 1 | a0003c0064t0005g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.178+6833G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406750 | ||||||
chr17:81406814
|
C | T | 92 | a0001c0003t0003g0044a0001c0003t0003g0047a0001c0003t0003g0048others(89): Show | 93 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.178+6897C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406814 | ||||||
chr17:81407361
|
G | T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+7444G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407361 | ||||||
chr17:81407640
|
G | A | 1 | a0001c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.178+7723G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407640 | ||||||
chr17:81407867
|
A | ACAACTGG others(8): Show |
1 | a0002c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.178+7951_178+7965d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81407867 | |||||
chr17:81407935
|
G | A | 16 | a0001c0007t0033g0135a0001c0009t0030g0263a0001c0021t0002g0262others(13): Show | 17 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+8018G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407935 | ||||||
chr17:81407955
|
C | T | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+8038C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407955 | ||||||
chr17:81408016
|
G | A | 1 | a0001c0003t0003g0286 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.178+8099G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408016 | ||||||
chr17:81408029
|
C | T | 1 | a0001c0009t0006g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.178+8112C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408029 | ||||||
chr17:81408042
|
C | T | 3 | a0004c0004t0002g0167a0004c0004t0002g0240a0004c0004t0002g0241 | 3 | HG00642.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.178+8125C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408042 | ||||||
chr17:81408074
|
C | A | 1 | a0010c0031t0004g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178+8157C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408074 | ||||||
chr17:81408117
|
G | C | 321 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(318): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.178+8200G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408117 | ||||||
chr17:81408210
|
G | A | 67 | a0001c0003t0003g0046a0001c0003t0003g0184a0001c0003t0003g0186others(64): Show | 69 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.178+8293G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408210 | ||||||
chr17:81408215
|
G | A | 3 | a0001c0007t0015g0275a0001c0009t0024g0248a0048c0045t0001g0254 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.178+8298G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408215 | ||||||
chr17:81408298
|
G | T | 14 | a0001c0009t0030g0263a0001c0021t0002g0262a0002c0001t0001g0274others(11): Show | 15 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+8381G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408298 | ||||||
chr17:81408486
|
C | T | 18 | a0001c0003t0003g0110a0001c0010t0004g0121a0002c0001t0001g0108others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+8569C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408486 | ||||||
chr17:81408563
|
G | A | 3 | a0004c0004t0002g0138a0004c0004t0002g0156a0004c0004t0022g0139 | 3 | HG03195.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.178+8646G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408563 | ||||||
chr17:81408616
|
C | T | 87 | a0001c0003t0003g0053a0001c0003t0003g0059a0001c0003t0003g0067others(84): Show | 88 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.178+8699C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408616 | ||||||
chr17:81408746
|
G | A | 1 | a0001c0003t0003g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178+8829G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408746 | ||||||
chr17:81408773
|
C | A | 1 | a0002c0016t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.178+8856C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408773 | ||||||
chr17:81408971
|
C | T | 3 | a0003c0002t0001g0039a0003c0002t0001g0095a0003c0002t0001g0096 | 3 | NA18948.hp1 NA18966.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.178+9054C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408971 | ||||||
chr17:81409038
|
C | T | 1 | a0001c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.178+9121C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409038 | ||||||
chr17:81409079
|
G | A | 14 | a0001c0009t0030g0263a0001c0021t0002g0262a0002c0001t0001g0274others(11): Show | 15 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+9162G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409079 | ||||||
chr17:81409159
|
A | G | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+9242A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409159 | ||||||
chr17:81409345
|
TG | T | 131 | a0001c0003t0003g0053a0001c0003t0003g0059a0001c0003t0003g0067others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.178+9433delG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81409345 | |||||
chr17:81409399
|
G | A | 1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+9482G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409399 | ||||||
chr17:81409406
|
G | C | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+9489G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409406 | ||||||
chr17:81409427
|
A | G | 4 | a0015c0014t0001g0243a0018c0106t0010g0328a0019c0105t0001g0249others(1): Show | 4 | HG00639.hp1 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+9510A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409427 | ||||||
chr17:81409434
|
C | T | 66 | a0001c0003t0003g0050a0001c0003t0003g0233a0001c0003t0003g0258others(63): Show | 67 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.178+9517C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409434 | ||||||
chr17:81409509
|
G | C | 3 | a0018c0106t0010g0328a0019c0105t0001g0249a0025c0107t0002g0250 | 3 | HG02486.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.178+9592G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409509 | ||||||
chr17:81409539
|
C | T | 2 | a0001c0010t0004g0121a0002c0001t0001g0113 | 2 | HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.178+9622C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409539 | ||||||
chr17:81409551
|
C | T | 6 | a0001c0009t0025g0252a0001c0069t0007g0253a0002c0001t0001g0274others(3): Show | 6 | HG01261.hp2 HG01884.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+9634C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409551 | ||||||
chr17:81409611
|
A | G | 11 | a0001c0003t0003g0231a0001c0012t0002g0133a0001c0012t0002g0159others(8): Show | 11 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+9694A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409611 | ||||||
chr17:81409650
|
C | T | 1 | a0001c0003t0003g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.178+9733C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409650 | ||||||
chr17:81409793
|
C | A | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+9876C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409793 | ||||||
chr17:81409804
|
G | T | 2 | a0001c0003t0003g0044a0003c0002t0004g0295 | 2 | NA18942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.178+9887G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409804 | ||||||
chr17:81409814
|
G | A | 73 | a0001c0003t0003g0047a0001c0003t0003g0048a0001c0003t0003g0059others(70): Show | 74 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.178+9897G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409814 | ||||||
chr17:81409814
|
G | C | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.178+9897G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409814 | ||||||
chr17:81409896
|
G | C | 2 | a0005c0065t0005g0179a0034c0033t0001g0178 | 2 | HG02523.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.178+9979G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409896 | ||||||
chr17:81409928
|
C | T | 1 | a0048c0045t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+10011C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409928 | ||||||
chr17:81409936
|
C | T | 1 | a0008c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178+10019C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409936 | ||||||
chr17:81410178
|
C | A | 1 | a0002c0081t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.178+10261C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410178 | ||||||
chr17:81410193
|
G | A | 1 | a0001c0007t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178+10276G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410193 | ||||||
chr17:81410221
|
C | G | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+10304C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410221 | ||||||
chr17:81410288
|
C | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+10371C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410288 | ||||||
chr17:81410288
|
C | G | 20 | a0001c0003t0010g0211a0001c0012t0002g0133a0001c0093t0001g0145others(17): Show | 20 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.178+10371C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410288 | ||||||
chr17:81410384
|
G | A | 1 | a0002c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+10467G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410384 | ||||||
chr17:81410423
|
G | A | 1 | a0016c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178+10506G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410423 | ||||||
chr17:81410461
|
T | C | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+10544T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410461 | ||||||
chr17:81410531
|
G | A | 1 | a0002c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+10614G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410531 | ||||||
chr17:81410535
|
C | T | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+10618C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410535 | ||||||
chr17:81410536
|
G | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+10619G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410536 | ||||||
chr17:81410539
|
G | A | 1 | a0016c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178+10622G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410539 | ||||||
chr17:81410590
|
G | C | 2 | a0002c0001t0001g0225a0005c0028t0001g0226 | 2 | NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.178+10673G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410590 | ||||||
chr17:81410591
|
A | T | 2 | a0002c0001t0001g0225a0005c0028t0001g0226 | 2 | NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.178+10674A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410591 | ||||||
chr17:81410591
|
AGGCACCA others(8): Show |
A | 3 | a0001c0019t0003g0315a0005c0005t0005g0202a0007c0008t0004g0317 | 3 | NA18983.hp1 NA19043.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.178+10701_178+1071 others(19): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81410591 | |||||
chr17:81410605
|
C | G | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+10688C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410605 | ||||||
chr17:81410606
|
T | A | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+10689T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410606 | ||||||
chr17:81410614
|
C | T | 2 | a0001c0012t0002g0058a0002c0001t0031g0196 | 2 | HG01358.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.178+10697C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410614 | ||||||
chr17:81410729
|
C | G | 28 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.178+10812C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410729 | ||||||
chr17:81410824
|
C | G | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+10907C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410824 | ||||||
chr17:81411019
|
A | G | 92 | a0001c0003t0003g0068a0001c0003t0003g0083a0001c0003t0003g0230others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.178+11102A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411019 | ||||||
chr17:81411236
|
G | A | 2 | a0015c0014t0001g0243a0016c0030t0007g0239 | 2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.178+11319G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411236 | ||||||
chr17:81411244
|
C | T | 82 | a0001c0003t0003g0068a0001c0003t0003g0083a0001c0003t0003g0231others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.178+11327C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411244 | ||||||
chr17:81411310
|
C | T | 4 | a0001c0009t0030g0263a0001c0021t0002g0262a0046c0047t0027g0264others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11393C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411310 | ||||||
chr17:81411346
|
A | G | 313 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(310): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.178+11429A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411346 | ||||||
chr17:81411351
|
C | T | 1 | a0001c0009t0025g0252 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.178+11434C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411351 | ||||||
chr17:81411474
|
C | CCCTG | 47 | a0001c0003t0003g0044a0001c0003t0003g0186a0001c0003t0003g0290others(44): Show | 47 | HG00544.hp1 HG00735.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.178+11597_178+1160 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
C | CCCTGCCT others(1): Show |
49 | a0001c0003t0003g0050a0001c0003t0003g0067a0001c0003t0003g0184others(46): Show | 50 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+11593_178+1160 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
C | CCCTGCCT others(5): Show |
13 | a0001c0003t0003g0047a0001c0003t0003g0048a0001c0012t0002g0133others(10): Show | 13 | HG02027.hp1 HG02071.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+11589_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
C | CCCTGCCT others(9): Show |
2 | a0001c0003t0003g0293a0003c0002t0004g0194 | 2 | HG00408.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.178+11585_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
C | CCCTGCCT others(13): Show |
1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+11581_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
C | CCCTGCCT others(17): Show |
1 | a0003c0002t0013g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178+11577_178+1160 others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
CCCTG | C | 5 | a0001c0009t0030g0263a0001c0009t0037g0319a0001c0021t0002g0262others(2): Show | 5 | HG02055.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+11597_178+1160 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
CCCTGCCT others(1): Show |
C | 9 | a0004c0004t0002g0003a0004c0004t0002g0266a0004c0004t0002g0269others(6): Show | 10 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.178+11593_178+1160 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411474
|
CCCTGCCT others(5): Show |
C | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+11589_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | |||||
chr17:81411490
|
GCCTGCCT others(33): Show |
G | 1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+11577_178+1161 others(44): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411490 | |||||
chr17:81411490
|
GCCTGCCT others(37): Show |
G | 2 | a0001c0007t0009g0260a0017c0023t0015g0277 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.178+11577_178+1162 others(48): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411490 | |||||
chr17:81411494
|
G | T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+11577G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411494 | ||||||
chr17:81411494
|
GCCTGCCT others(29): Show |
G | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+11581_178+1161 others(40): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411494 | |||||
chr17:81411494
|
GCCTGCCT others(33): Show |
G | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+11581_178+1162 others(44): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411494 | |||||
chr17:81411502
|
GCCTGCCT others(9): Show |
G | 1 | a0002c0001t0001g0091 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.178+11589_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411502 | |||||
chr17:81411502
|
GCCTGCCT others(13): Show |
G | 2 | a0001c0007t0016g0234a0017c0023t0038g0027 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.178+11589_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411502 | |||||
chr17:81411502
|
GCCTGCCT others(21): Show |
G | 1 | a0013c0027t0001g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.178+11589_178+1161 others(32): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411502 | |||||
chr17:81411506
|
GCCTGCCT others(5): Show |
G | 1 | a0052c0038t0002g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178+11593_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411506 | |||||
chr17:81411506
|
GCCTGCCT others(13): Show |
G | 14 | a0001c0009t0025g0252a0001c0012t0002g0137a0001c0069t0007g0253others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+11593_178+1161 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411506 | |||||
chr17:81411506
|
GCCTGCCT others(17): Show |
G | 1 | a0013c0027t0001g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178+11593_178+1161 others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411506 | |||||
chr17:81411510
|
GCCTGCCT others(5): Show |
G | 2 | a0001c0009t0024g0248a0007c0008t0001g0257 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.178+11597_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411510 | |||||
chr17:81411510
|
GCCTGCCT others(9): Show |
G | 3 | a0001c0003t0003g0233a0003c0018t0002g0143a0057c0104t0010g0160 | 3 | HG00642.hp2 HG01175.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.178+11597_178+1161 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411510 | |||||
chr17:81411514
|
G | GCCTGCCT others(13): Show |
2 | a0001c0093t0001g0145a0035c0095t0002g0146 | 2 | HG00733.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178+11600_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTGCCT others(9): Show |
1 | a0029c0070t0003g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.178+11600_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTGCCT others(5): Show |
3 | a0001c0003t0003g0059a0001c0092t0004g0227a0005c0096t0005g0199 | 3 | HG01943.hp1 NA18963.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.178+11600_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTGCCT others(13): Show |
1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+11600_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTGCCT others(17): Show |
1 | a0034c0033t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.178+11600_178+1160 others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTGCCT others(1): Show |
4 | a0001c0003t0003g0046a0002c0016t0001g0181a0006c0006t0001g0201others(1): Show | 4 | HG00673.hp1 HG01192.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11600_178+1160 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTGCCT others(9): Show |
1 | a0001c0003t0003g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.178+11600_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTT | 8 | a0001c0003t0003g0047a0001c0003t0003g0048a0001c0003t0003g0230others(5): Show | 8 | HG00544.hp1 HG01516.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+11654_178+1165 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTTCCT others(1): Show |
4 | a0001c0007t0002g0007a0002c0001t0001g0291a0002c0001t0002g0177others(1): Show | 4 | HG02683.hp2 HG03491.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11650_178+1165 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | GCCTTCCT others(5): Show |
2 | a0003c0002t0004g0280a0023c0084t0003g0129 | 2 | HG03490.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.178+11646_178+1165 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
G | T | 2 | a0001c0094t0009g0016a0014c0022t0036g0318 | 2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.178+11597G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411514 | ||||||
chr17:81411514
|
GCCTT | G | 70 | a0001c0003t0003g0044a0001c0003t0003g0068a0001c0003t0003g0083others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.178+11654_178+1165 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
GCCTTCCT others(1): Show |
G | 29 | a0001c0003t0003g0053a0001c0003t0003g0231a0001c0010t0001g0034others(26): Show | 32 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.178+11650_178+1165 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
GCCTTCCT others(5): Show |
G | 20 | a0001c0003t0003g0110a0001c0007t0033g0135a0001c0009t0030g0263others(17): Show | 20 | HG00609.hp2 HG00639.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.178+11646_178+1165 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
GCCTTCCT others(9): Show |
G | 15 | a0001c0003t0003g0302a0001c0009t0037g0319a0001c0026t0003g0246others(12): Show | 15 | HG01243.hp2 HG02055.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.178+11642_178+1165 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411514
|
GCCTTCCT others(13): Show |
G | 3 | a0002c0001t0001g0320a0006c0020t0002g0325a0007c0008t0004g0317 | 3 | HG01074.hp2 HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178+11638_178+1165 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | |||||
chr17:81411518
|
T | G | 70 | a0001c0003t0003g0186a0001c0003t0003g0286a0001c0003t0003g0290others(67): Show | 70 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.178+11601T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411518 | ||||||
chr17:81411522
|
T | G | 46 | a0001c0003t0003g0286a0001c0007t0015g0275a0001c0010t0004g0121others(43): Show | 46 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.178+11605T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411522 | ||||||
chr17:81411526
|
T | G | 22 | a0001c0003t0003g0053a0001c0007t0015g0275a0001c0010t0001g0034others(19): Show | 24 | HG00544.hp2 HG01168.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.178+11609T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411526 | ||||||
chr17:81411530
|
T | G | 23 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0007t0033g0135others(20): Show | 24 | HG00609.hp2 HG00639.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.178+11613T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411530 | ||||||
chr17:81411534
|
T | G | 1 | a0048c0045t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+11617T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411534 | ||||||
chr17:81411566
|
T | C | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+11649T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411566 | ||||||
chr17:81411577
|
G | C | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178+11660G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411577 | ||||||
chr17:81411952
|
C | T | 2 | a0002c0001t0001g0276a0016c0030t0007g0032 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.178+12035C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411952 | ||||||
chr17:81411966
|
G | A | 1 | a0003c0002t0001g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.178+12049G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411966 | ||||||
chr17:81412074
|
G | A | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+12157G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412074 | ||||||
chr17:81412151
|
C | T | 2 | a0002c0001t0001g0274a0016c0030t0007g0239 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.178+12234C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412151 | ||||||
chr17:81412169
|
C | T | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178+12252C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412169 | ||||||
chr17:81412187
|
C | T | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.178+12270C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412187 | ||||||
chr17:81412305
|
T | C | 28 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.178+12388T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412305 | ||||||
chr17:81412491
|
T | G | 1 | a0001c0085t0001g0073 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.178+12574T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412491 | ||||||
chr17:81412494
|
G | A | 6 | a0002c0001t0001g0176a0003c0002t0004g0182a0003c0002t0004g0194others(3): Show | 6 | HG02738.hp1 HG03491.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+12577G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412494 | ||||||
chr17:81412628
|
C | T | 1 | a0007c0008t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178+12711C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412628 | ||||||
chr17:81412662
|
G | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+12745G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412662 | ||||||
chr17:81412698
|
C | T | 1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+12781C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412698 | ||||||
chr17:81412789
|
T | C | 1 | a0019c0105t0001g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.178+12872T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412789 | ||||||
chr17:81412793
|
A | T | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+12876A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412793 | ||||||
chr17:81412854
|
T | C | 1 | a0024c0082t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.178+12937T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412854 | ||||||
chr17:81412953
|
A | C | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+13036A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412953 | ||||||
chr17:81412956
|
G | A | 1 | a0001c0099t0003g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.178+13039G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412956 | ||||||
chr17:81412962
|
C | T | 3 | a0001c0009t0025g0252a0001c0069t0007g0253a0002c0063t0020g0251 | 3 | HG01261.hp2 HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.178+13045C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412962 | ||||||
chr17:81412981
|
C | T | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.178+13064C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412981 | ||||||
chr17:81413059
|
C | T | 44 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(41): Show | 45 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.178+13142C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413059 | ||||||
chr17:81413144
|
G | A | 1 | a0030c0090t0002g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.178+13227G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413144 | ||||||
chr17:81413152
|
A | G | 28 | a0001c0003t0003g0184a0001c0009t0025g0252a0001c0009t0037g0319others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.178+13235A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413152 | ||||||
chr17:81413214
|
G | C | 4 | a0002c0001t0001g0030a0002c0001t0002g0177a0002c0001t0005g0064others(1): Show | 4 | HG02683.hp2 HG03654.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+13297G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413214 | ||||||
chr17:81413258
|
G | A | 1 | a0012c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178+13341G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413258 | ||||||
chr17:81413329
|
G | T | 1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+13412G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413329 | ||||||
chr17:81413400
|
C | T | 1 | a0024c0082t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.179-13400C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413400 | ||||||
chr17:81413413
|
G | C | 2 | a0002c0001t0001g0274a0016c0030t0007g0239 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.179-13387G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413413 | ||||||
chr17:81413493
|
C | T | 1 | a0004c0004t0002g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.179-13307C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413493 | ||||||
chr17:81413571
|
G | A | 5 | a0001c0007t0009g0260a0013c0097t0001g0235a0016c0030t0007g0032others(2): Show | 5 | HG00099.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-13229G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413571 | ||||||
chr17:81413603
|
C | A | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-13197C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413603 | ||||||
chr17:81413651
|
C | T | 50 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(47): Show | 51 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.179-13149C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413651 | ||||||
chr17:81413683
|
G | A | 1 | a0002c0062t0007g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.179-13117G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413683 | ||||||
chr17:81413692
|
C | G | 317 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(314): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.179-13108C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413692 | ||||||
chr17:81413695
|
G | T | 4 | a0001c0012t0002g0058a0001c0012t0002g0159a0002c0001t0031g0196others(1): Show | 4 | HG01346.hp2 HG01358.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-13105G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413695 | ||||||
chr17:81413736
|
C | G | 217 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.179-13064C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413736 | ||||||
chr17:81413744
|
G | A | 4 | a0001c0003t0003g0067a0004c0004t0002g0167a0004c0004t0002g0240others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-13056G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413744 | ||||||
chr17:81413750
|
G | A | 29 | a0001c0003t0003g0184a0001c0009t0025g0252a0001c0009t0037g0319others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-13050G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413750 | ||||||
chr17:81413842
|
G | A | 6 | a0001c0007t0009g0260a0002c0001t0001g0274a0007c0008t0004g0317others(3): Show | 6 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-12958G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413842 | ||||||
chr17:81413853
|
C | T | 2 | a0001c0007t0016g0234a0017c0023t0038g0027 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.179-12947C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413853 | ||||||
chr17:81413933
|
C | T | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.179-12867C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413933 | ||||||
chr17:81413934
|
G | A | 1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-12866G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413934 | ||||||
chr17:81413977
|
C | G | 1 | a0001c0009t0004g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.179-12823C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413977 | ||||||
chr17:81414069
|
C | T | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-12731C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414069 | ||||||
chr17:81414084
|
G | T | 2 | a0001c0007t0009g0260a0017c0023t0015g0277 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-12716G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414084 | ||||||
chr17:81414232
|
G | A | 12 | a0001c0010t0009g0185a0002c0001t0001g0169a0002c0001t0001g0174others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-12568G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414232 | ||||||
chr17:81414582
|
C | T | 1 | a0048c0045t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.179-12218C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414582 | ||||||
chr17:81414678
|
G | C | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-12122G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414678 | ||||||
chr17:81414717
|
G | A | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-12083G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414717 | ||||||
chr17:81414722
|
G | A | 3 | a0001c0007t0015g0275a0002c0001t0001g0276a0016c0030t0007g0032 | 3 | HG02723.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.179-12078G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414722 | ||||||
chr17:81414890
|
C | T | 1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-11910C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414890 | ||||||
chr17:81414949
|
C | T | 44 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(41): Show | 45 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.179-11851C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414949 | ||||||
chr17:81414992
|
G | T | 1 | a0016c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.179-11808G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414992 | ||||||
chr17:81415004
|
C | T | 3 | a0001c0025t0003g0212a0002c0001t0001g0274a0016c0030t0007g0239 | 3 | HG02015.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.179-11796C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415004 | ||||||
chr17:81415015
|
G | A | 1 | a0041c0053t0001g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.179-11785G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415015 | ||||||
chr17:81415070
|
CG | C | 32 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0010t0009g0185others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-11728delG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81415070 | |||||
chr17:81415123
|
G | A | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-11677G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415123 | ||||||
chr17:81415310
|
C | G | 1 | a0004c0011t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.179-11490C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415310 | ||||||
chr17:81415359
|
G | A | 1 | a0001c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179-11441G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415359 | ||||||
chr17:81415371
|
G | A | 4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-11429G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415371 | ||||||
chr17:81415446
|
G | A | 1 | a0002c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.179-11354G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415446 | ||||||
chr17:81415451
|
C | T | 299 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(296): Show | 302 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.179-11349C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415451 | ||||||
chr17:81415611
|
C | T | 12 | a0001c0012t0002g0137a0003c0018t0002g0143a0004c0004t0002g0092others(9): Show | 12 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-11189C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415611 | ||||||
chr17:81415667
|
G | T | 2 | a0001c0007t0009g0260a0017c0023t0015g0277 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-11133G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415667 | ||||||
chr17:81415686
|
G | A | 225 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.179-11114G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415686 | ||||||
chr17:81415692
|
G | A | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-11108G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415692 | ||||||
chr17:81415749
|
G | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-11051G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415749 | ||||||
chr17:81415861
|
C | T | 2 | a0001c0019t0003g0315a0005c0005t0005g0202 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-10939C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415861 | ||||||
chr17:81415879
|
C | T | 12 | a0001c0007t0015g0275a0001c0069t0007g0253a0002c0001t0001g0169others(9): Show | 12 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-10921C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415879 | ||||||
chr17:81415935
|
C | G | 1 | a0004c0004t0002g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.179-10865C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415935 | ||||||
chr17:81415944
|
A | G | 5 | a0001c0007t0015g0275a0001c0069t0007g0253a0002c0001t0001g0276others(2): Show | 5 | HG00639.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-10856A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415944 | ||||||
chr17:81416007
|
CGT | C | 5 | a0001c0007t0009g0260a0004c0011t0002g0162a0009c0013t0006g0163others(2): Show | 5 | HG01074.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-10782_179-1078 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416007 | |||||
chr17:81416009
|
T | C | 2 | a0001c0019t0003g0315a0005c0005t0005g0202 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-10791T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416009 | ||||||
chr17:81416011
|
T | C | 2 | a0005c0005t0008g0297a0005c0005t0008g0298 | 2 | HG01069.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.179-10789T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416011 | ||||||
chr17:81416011
|
TGTGTGTG others(31): Show |
T | 3 | a0002c0001t0001g0274a0016c0030t0007g0032a0016c0030t0007g0239 | 3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-10761_179-1072 others(42): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416011 | |||||
chr17:81416051
|
T | C | 3 | a0002c0001t0001g0274a0016c0030t0007g0032a0016c0030t0007g0239 | 3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-10749T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416051 | ||||||
chr17:81416065
|
G | A | 42 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.179-10735G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416065 | ||||||
chr17:81416074
|
A | G | 1 | a0003c0002t0004g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.179-10726A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416074 | ||||||
chr17:81416087
|
C | T | 1 | a0001c0012t0002g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.179-10713C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416087 | ||||||
chr17:81416107
|
GGTGT | G | 42 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.179-10684_179-1068 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416107 | |||||
chr17:81416248
|
G | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-10552G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416248 | ||||||
chr17:81416253
|
C | T | 1 | a0002c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.179-10547C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416253 | ||||||
chr17:81416317
|
C | T | 2 | a0013c0027t0001g0025a0013c0027t0001g0026 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-10483C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416317 | ||||||
chr17:81416397
|
C | T | 5 | a0001c0010t0009g0185a0002c0001t0001g0327a0010c0031t0004g0018others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-10403C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416397 | ||||||
chr17:81416439
|
CGT | C | 9 | a0001c0103t0026g0245a0002c0001t0006g0148a0002c0001t0007g0147others(6): Show | 9 | HG00738.hp1 HG02300.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-10350_179-1034 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416439 | |||||
chr17:81416460
|
G | GGT | 5 | a0001c0007t0016g0234a0001c0094t0009g0016a0004c0011t0002g0023others(2): Show | 5 | HG02109.hp1 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-10321_179-1032 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416460 | |||||
chr17:81416477
|
G | GTATGTGT others(63): Show |
1 | a0002c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.179-10322_179-1032 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTCCATGA others(57): Show |
4 | a0018c0106t0010g0328a0019c0105t0001g0249a0025c0107t0002g0250others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-10322_179-1032 others(68): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTCC others(71): Show |
1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-10320_179-1031 others(82): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTCC others(69): Show |
6 | a0001c0101t0010g0020a0002c0001t0001g0324a0002c0001t0001g0326others(3): Show | 6 | HG01074.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(80): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTCC others(61): Show |
6 | a0001c0010t0004g0121a0002c0001t0007g0147a0002c0016t0001g0052others(3): Show | 6 | HG00738.hp1 HG01978.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(72): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTCC others(71): Show |
72 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(69): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(82): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(63): Show |
1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-10320_179-1031 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(61): Show |
1 | a0038c0059t0002g0008 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.179-10320_179-1031 others(72): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(63): Show |
196 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(73): Show |
4 | a0001c0007t0009g0260a0003c0002t0013g0024a0013c0097t0001g0235others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(84): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(63): Show |
2 | a0001c0003t0003g0230a0056c0100t0001g0237 | 2 | NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.179-10320_179-1031 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(65): Show |
11 | a0001c0010t0004g0296a0002c0001t0001g0004a0002c0001t0001g0088others(8): Show | 13 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(76): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416477
|
G | GTGTGTGT others(77): Show |
1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-10320_179-1031 others(88): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | |||||
chr17:81416498
|
T | TGC | 305 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(302): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.179-10301_179-1030 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | |||||
chr17:81416498
|
T | TGCGTGTG others(69): Show |
1 | a0002c0001t0001g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.179-10300_179-1029 others(80): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | |||||
chr17:81416498
|
T | TGCGTGTG others(69): Show |
2 | a0001c0019t0003g0315a0005c0005t0005g0202 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-10300_179-1029 others(80): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | |||||
chr17:81416498
|
T | TGCGTGTG others(61): Show |
4 | a0001c0099t0003g0051a0002c0001t0001g0037a0002c0001t0001g0136others(1): Show | 4 | HG00438.hp1 HG02074.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-10300_179-1029 others(72): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | |||||
chr17:81416498
|
T | TGCGTGTG others(71): Show |
6 | a0001c0009t0024g0248a0001c0026t0003g0247a0007c0008t0001g0257others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-10300_179-1029 others(82): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | |||||
chr17:81416570
|
CGT | C | 226 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(223): Show | 228 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.179-10219_179-1021 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416570 | |||||
chr17:81416601
|
C | T | 1 | a0001c0101t0010g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179-10199C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416601 | ||||||
chr17:81416604
|
G | A | 1 | a0002c0052t0001g0045 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.179-10196G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416604 | ||||||
chr17:81416605
|
T | C | 1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-10195T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416605 | ||||||
chr17:81416612
|
G | A | 1 | a0016c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.179-10188G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416612 | ||||||
chr17:81416624
|
A | C | 1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-10176A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416624 | ||||||
chr17:81416708
|
C | T | 31 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0010t0009g0185others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-10092C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416708 | ||||||
chr17:81416726
|
C | T | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-10074C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416726 | ||||||
chr17:81416926
|
C | T | 1 | a0001c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179-9874C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416926 | ||||||
chr17:81417122
|
G | C | 4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-9678G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417122 | ||||||
chr17:81417153
|
G | A | 5 | a0002c0001t0001g0035a0002c0001t0001g0036a0002c0001t0001g0203others(2): Show | 5 | HG00408.hp2 HG02886.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-9647G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417153 | ||||||
chr17:81417164
|
C | T | 1 | a0001c0003t0003g0300 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.179-9636C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417164 | ||||||
chr17:81417179
|
G | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-9621G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417179 | ||||||
chr17:81417195
|
C | T | 1 | a0001c0003t0003g0046 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.179-9605C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417195 | ||||||
chr17:81417268
|
G | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-9532G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417268 | ||||||
chr17:81417274
|
C | T | 3 | a0001c0007t0009g0260a0013c0097t0001g0235a0017c0023t0015g0277 | 3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-9526C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417274 | ||||||
chr17:81417300
|
T | TGGTTGCA others(7): Show |
1 | a0003c0002t0004g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.179-9498_179-9485d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417300 | |||||
chr17:81417398
|
G | A | 1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.179-9402G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417398 | ||||||
chr17:81417423
|
A | G | 2 | a0007c0008t0004g0317a0047c0046t0004g0273 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.179-9377A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417423 | ||||||
chr17:81417514
|
G | A | 2 | a0001c0019t0003g0315a0005c0005t0005g0202 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-9286G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417514 | ||||||
chr17:81417555
|
A | AC | 32 | a0001c0007t0009g0260a0001c0009t0037g0319a0001c0012t0002g0137others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-9235dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | |||||
chr17:81417555
|
A | ACC | 36 | a0001c0003t0003g0302a0001c0007t0009g0014a0001c0007t0016g0161others(33): Show | 37 | HG00609.hp2 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.179-9236_179-9235d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | |||||
chr17:81417555
|
A | ACCG | 94 | a0001c0003t0003g0044a0001c0003t0003g0048a0001c0003t0003g0068others(91): Show | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.179-9243_179-9242i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | |||||
chr17:81417555
|
A | ACCGC | 25 | a0001c0003t0003g0047a0001c0009t0006g0134a0001c0010t0004g0121others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.179-9243_179-9242i others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | |||||
chr17:81417560
|
C | CCCG | 103 | a0001c0003t0003g0046a0001c0003t0003g0050a0001c0003t0003g0059others(100): Show | 104 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.179-9238_179-9237i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417560 | |||||
chr17:81417686
|
G | C | 319 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(316): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.179-9114G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417686 | ||||||
chr17:81417945
|
C | T | 2 | a0007c0008t0004g0317a0047c0046t0004g0273 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.179-8855C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417945 | ||||||
chr17:81418125
|
C | T | 2 | a0001c0019t0003g0315a0005c0005t0005g0202 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-8675C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418125 | ||||||
chr17:81418170
|
C | T | 2 | a0001c0069t0007g0253a0002c0001t0001g0276 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.179-8630C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418170 | ||||||
chr17:81418199
|
C | T | 1 | a0001c0003t0003g0067 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.179-8601C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418199 | ||||||
chr17:81418265
|
G | A | 3 | a0001c0007t0009g0014a0001c0007t0016g0161a0001c0009t0024g0248 | 3 | HG02630.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.179-8535G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418265 | ||||||
chr17:81418289
|
T | C | 27 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-8511T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418289 | ||||||
chr17:81418533
|
C | T | 1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-8267C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418533 | ||||||
chr17:81418538
|
C | T | 11 | a0001c0012t0002g0137a0004c0004t0002g0092a0004c0004t0002g0093others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.179-8262C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418538 | ||||||
chr17:81418568
|
C | T | 3 | a0001c0007t0009g0260a0013c0097t0001g0235a0017c0023t0015g0277 | 3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-8232C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418568 | ||||||
chr17:81418617
|
G | C | 4 | a0018c0106t0010g0328a0019c0105t0001g0249a0025c0107t0002g0250others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-8183G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418617 | ||||||
chr17:81418632
|
A | G | 2 | a0007c0008t0004g0317a0047c0046t0004g0273 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.179-8168A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418632 | ||||||
chr17:81418688
|
C | T | 1 | a0012c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.179-8112C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418688 | ||||||
chr17:81418697
|
C | T | 1 | a0003c0002t0004g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.179-8103C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418697 | ||||||
chr17:81418766
|
C | CGT | 33 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.179-8027_179-8026d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418766 | |||||
chr17:81418774
|
T | C | 1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-8026T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418774 | ||||||
chr17:81418775
|
A | G | 1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-8025A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418775 | ||||||
chr17:81418776
|
C | CGTGTGTG others(3): Show |
1 | a0009c0013t0006g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.179-8017_179-8016i others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418776 | |||||
chr17:81418776
|
C | T | 1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-8024C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418776 | ||||||
chr17:81418776
|
CGT | C | 3 | a0001c0007t0033g0135a0001c0025t0003g0212a0004c0037t0014g0256 | 3 | HG02015.hp2 HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.179-8015_179-8014d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418776 | |||||
chr17:81418777
|
G | A | 1 | a0002c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.179-8023G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418777 | ||||||
chr17:81418782
|
T | TGC | 29 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-8017_179-8016i others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418782 | |||||
chr17:81418784
|
T | C | 3 | a0002c0001t0001g0274a0016c0030t0007g0032a0016c0030t0007g0239 | 3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-8016T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418784 | ||||||
chr17:81418787
|
A | G | 35 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.179-8013A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418787 | ||||||
chr17:81418788
|
C | T | 32 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-8012C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418788 | ||||||
chr17:81418794
|
T | C | 3 | a0002c0001t0001g0274a0016c0030t0007g0032a0016c0030t0007g0239 | 3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-8006T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418794 | ||||||
chr17:81418795
|
G | GTGTGCGC others(3): Show |
1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-8005_179-8004i others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418795 | ||||||
chr17:81418795
|
GCGTGTGT others(7): Show |
G | 3 | a0001c0007t0009g0014a0001c0007t0016g0161a0015c0014t0001g0243 | 3 | HG00639.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.179-7991_179-7978d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418795 | |||||
chr17:81418796
|
C | CGCGCAT | 27 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-8003_179-8002i others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | |||||
chr17:81418796
|
C | CGCGCATG others(17): Show |
1 | a0002c0074t0001g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.179-8003_179-8002i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | |||||
chr17:81418796
|
C | CGTGCAT | 3 | a0002c0001t0001g0274a0016c0030t0007g0032a0016c0030t0007g0239 | 3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-8001_179-8000i others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | |||||
chr17:81418796
|
C | CGTGTGCG others(5): Show |
1 | a0001c0021t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.179-7999_179-7998i others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | |||||
chr17:81418796
|
C | CGTGTGTG others(11): Show |
4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-7993_179-7992i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | |||||
chr17:81418796
|
C | CGTGTGTG others(13): Show |
16 | a0001c0007t0015g0275a0001c0009t0004g0117a0001c0009t0030g0263others(13): Show | 16 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-7992_179-7991i others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | |||||
chr17:81418796
|
C | T | 3 | a0001c0103t0026g0245a0009c0013t0006g0163a0045c0080t0004g0128 | 3 | HG01516.hp1 HG02615.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.179-8004C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418796 | ||||||
chr17:81418797
|
G | GTGTGTGT others(9): Show |
1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-7993_179-7992i others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418797 | |||||
chr17:81418797
|
G | GTGTGTGT others(11): Show |
6 | a0001c0009t0024g0248a0003c0002t0004g0310a0007c0008t0001g0309others(3): Show | 6 | HG01243.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-7992_179-7991i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418797 | |||||
chr17:81418799
|
G | A | 1 | a0004c0011t0002g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.179-8001G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418799 | ||||||
chr17:81418804
|
T | TGTGCGCG others(17): Show |
2 | a0001c0021t0002g0077a0001c0021t0002g0114 | 2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.179-7993_179-7992i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418804 | |||||
chr17:81418804
|
T | TGTGTGTG others(19): Show |
1 | a0001c0007t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.179-7992_179-7991i others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418804 | |||||
chr17:81418804
|
T | TGTGTGTG others(21): Show |
1 | a0034c0033t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.179-7992_179-7991i others(30): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418804 | |||||
chr17:81418806
|
T | TGTGTGCG others(17): Show |
3 | a0001c0093t0001g0145a0035c0095t0002g0146a0055c0034t0002g0216 | 3 | HG00733.hp1 HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.179-7992_179-7991i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418806 | |||||
chr17:81418808
|
T | C | 3 | a0001c0007t0009g0260a0013c0097t0001g0235a0017c0023t0015g0277 | 3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-7992T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418808 | ||||||
chr17:81418809
|
A | G | 253 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(250): Show | 256 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.179-7991A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418809 | ||||||
chr17:81418810
|
C | CGCATGTG others(17): Show |
1 | a0011c0015t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(5): Show |
1 | a0002c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-7989_179-7988i others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(11): Show |
2 | a0001c0019t0003g0315a0005c0005t0005g0202 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-7989_179-7988i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(13): Show |
1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-7989_179-7988i others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(15): Show |
7 | a0001c0003t0003g0110a0001c0003t0003g0302a0001c0012t0002g0112others(4): Show | 7 | HG02083.hp1 HG02132.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(17): Show |
28 | a0001c0003t0003g0050a0001c0003t0003g0053a0001c0003t0003g0258others(25): Show | 29 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(19): Show |
1 | a0002c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(15): Show |
12 | a0001c0003t0003g0314a0002c0001t0031g0196a0002c0072t0001g0080others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(17): Show |
23 | a0001c0003t0010g0211a0001c0012t0002g0133a0002c0001t0001g0242others(20): Show | 23 | HG00738.hp1 HG01070.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(19): Show |
147 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(144): Show | 149 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(21): Show |
10 | a0001c0012t0002g0058a0001c0012t0002g0159a0001c0019t0003g0200others(7): Show | 10 | HG01346.hp2 HG01952.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(30): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCATG others(23): Show |
1 | a0003c0018t0002g0210 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(32): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCGTG others(13): Show |
1 | a0002c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCGTG others(11): Show |
1 | a0001c0101t0010g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179-7989_179-7988i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGCGCGTG others(15): Show |
5 | a0002c0001t0001g0326a0002c0001t0001g0327a0006c0020t0002g0325others(2): Show | 5 | HG01074.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGT | 3 | a0001c0103t0026g0245a0017c0023t0038g0027a0047c0046t0004g0273 | 3 | HG02615.hp1 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.179-7969_179-7968d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGTGT | 4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-7971_179-7968d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGTGTGTG others(3): Show |
11 | a0001c0009t0025g0252a0003c0002t0013g0024a0003c0018t0002g0143others(8): Show | 12 | HG00140.hp2 HG00642.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-7977_179-7968d others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGTGTGTG others(5): Show |
6 | a0001c0009t0037g0319a0001c0012t0002g0137a0004c0004t0002g0218others(3): Show | 6 | HG00099.hp1 HG01074.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-7979_179-7968d others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | CGTGTGTG others(7): Show |
6 | a0004c0004t0002g0092a0004c0004t0002g0093a0004c0004t0014g0190others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-7981_179-7968d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418810
|
C | T | 9 | a0001c0007t0033g0135a0001c0021t0002g0077a0001c0021t0002g0114others(6): Show | 9 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-7990C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418810 | ||||||
chr17:81418810
|
CGT | C | 3 | a0001c0021t0002g0262a0001c0094t0009g0016a0002c0001t0001g0274 | 3 | HG02886.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.179-7969_179-7968d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | |||||
chr17:81418811
|
G | GCATGTGT others(9): Show |
3 | a0001c0007t0009g0260a0013c0097t0001g0235a0017c0023t0015g0277 | 3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-7989_179-7988i others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418811 | ||||||
chr17:81418812
|
T | C | 3 | a0001c0007t0009g0260a0013c0097t0001g0235a0017c0023t0015g0277 | 3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-7988T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418812 | ||||||
chr17:81418834
|
G | T | 4 | a0003c0002t0001g0039a0003c0002t0001g0095a0003c0002t0001g0096others(1): Show | 4 | NA18948.hp1 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-7966G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418834 | ||||||
chr17:81418882
|
A | G | 3 | a0002c0001t0001g0274a0016c0030t0007g0032a0016c0030t0007g0239 | 3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-7918A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418882 | ||||||
chr17:81418958
|
C | CTGTGCAA others(9): Show |
1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-7811_179-7796d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418958 | |||||
chr17:81419399
|
G | GAATGTGG others(54): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-7400_179-7340d others(63): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81419399 | |||||
chr17:81419421
|
G | T | 43 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(40): Show | 44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.179-7379G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419421 | ||||||
chr17:81419516
|
C | T | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-7284C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419516 | ||||||
chr17:81419566
|
C | T | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-7234C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419566 | ||||||
chr17:81419567
|
G | A | 1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-7233G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419567 | ||||||
chr17:81419788
|
C | CT | 73 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(70): Show | 74 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.179-7012_179-7011i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419788 | ||||||
chr17:81419788
|
C | CTT | 3 | a0001c0003t0003g0067a0023c0084t0003g0129a0033c0067t0001g0305 | 3 | HG01433.hp2 HG01943.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.179-7012_179-7011i others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419788 | ||||||
chr17:81419788
|
CG | C | 7 | a0001c0009t0004g0117a0002c0001t0001g0035a0007c0048t0002g0308others(4): Show | 7 | HG01255.hp2 HG01516.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-7011delG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419788 | ||||||
chr17:81419789
|
G | T | 316 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(313): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.179-7011G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419789 | ||||||
chr17:81419835
|
A | G | 8 | a0004c0004t0002g0003a0004c0004t0002g0266a0004c0004t0002g0269others(5): Show | 9 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-6965A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419835 | ||||||
chr17:81419882
|
C | T | 2 | a0004c0004t0002g0221a0004c0004t0002g0222 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.179-6918C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419882 | ||||||
chr17:81419924
|
C | T | 4 | a0018c0106t0010g0328a0019c0105t0001g0249a0025c0107t0002g0250others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-6876C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419924 | ||||||
chr17:81419963
|
A | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-6837A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419963 | ||||||
chr17:81420069
|
C | T | 1 | a0002c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-6731C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420069 | ||||||
chr17:81420221
|
C | T | 27 | a0001c0007t0009g0260a0001c0009t0025g0252a0001c0009t0037g0319others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-6579C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420221 | ||||||
chr17:81420319
|
A | C | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-6481A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420319 | ||||||
chr17:81420410
|
C | A | 1 | a0001c0012t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.179-6390C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420410 | ||||||
chr17:81420412
|
C | T | 1 | a0040c0054t0001g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.179-6388C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420412 | ||||||
chr17:81420488
|
T | C | 1 | a0002c0001t0001g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.179-6312T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420488 | ||||||
chr17:81420496
|
C | T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-6304C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420496 | ||||||
chr17:81420673
|
A | G | 1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-6127A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420673 | ||||||
chr17:81420710
|
G | T | 2 | a0001c0009t0024g0248a0047c0046t0004g0273 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.179-6090G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420710 | ||||||
chr17:81420736
|
A | G | 282 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(279): Show | 285 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.179-6064A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420736 | ||||||
chr17:81420760
|
C | T | 4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-6040C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420760 | ||||||
chr17:81420778
|
C | T | 2 | a0002c0001t0001g0320a0014c0022t0036g0318 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.179-6022C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420778 | ||||||
chr17:81420813
|
C | G | 6 | a0001c0086t0003g0031a0002c0044t0001g0164a0003c0002t0001g0124others(3): Show | 6 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-5987C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420813 | ||||||
chr17:81420828
|
C | G | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-5972C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420828 | ||||||
chr17:81420892
|
A | C | 1 | a0003c0002t0004g0280 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.179-5908A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420892 | ||||||
chr17:81421018
|
C | T | 4 | a0002c0001t0001g0030a0002c0001t0002g0177a0002c0001t0005g0064others(1): Show | 4 | HG02683.hp2 HG03654.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-5782C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421018 | ||||||
chr17:81421252
|
A | G | 322 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(319): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.179-5548A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421252 | ||||||
chr17:81421438
|
C | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-5362C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421438 | ||||||
chr17:81421531
|
G | A | 1 | a0002c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.179-5269G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421531 | ||||||
chr17:81421554
|
C | T | 1 | a0050c0043t0004g0060 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.179-5246C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421554 | ||||||
chr17:81421695
|
C | T | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-5105C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421695 | ||||||
chr17:81421762
|
C | T | 220 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(217): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.179-5038C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421762 | ||||||
chr17:81421763
|
G | A | 3 | a0001c0094t0009g0016a0010c0031t0004g0015a0030c0090t0002g0265 | 3 | HG02895.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.179-5037G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421763 | ||||||
chr17:81421821
|
C | T | 43 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(40): Show | 44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.179-4979C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421821 | ||||||
chr17:81421889
|
G | A | 43 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(40): Show | 44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.179-4911G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421889 | ||||||
chr17:81421908
|
T | C | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-4892T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421908 | ||||||
chr17:81421967
|
C | T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-4833C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421967 | ||||||
chr17:81421983
|
G | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-4817G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421983 | ||||||
chr17:81422014
|
A | AT | 220 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(217): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.179-4775dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81422014 | |||||
chr17:81422014
|
AT | A | 24 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(21): Show | 25 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.179-4775delT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81422014 | |||||
chr17:81422029
|
G | T | 1 | a0017c0023t0015g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179-4771G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422029 | ||||||
chr17:81422035
|
G | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-4765G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422035 | ||||||
chr17:81422041
|
G | A | 1 | a0001c0007t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.179-4759G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422041 | ||||||
chr17:81422124
|
G | A | 1 | a0001c0003t0003g0184 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.179-4676G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422124 | ||||||
chr17:81422159
|
G | A | 3 | a0001c0019t0003g0315a0005c0005t0005g0202a0005c0096t0005g0199 | 3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-4641G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422159 | ||||||
chr17:81422509
|
C | T | 1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-4291C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422509 | ||||||
chr17:81422631
|
C | T | 2 | a0007c0008t0001g0257a0017c0023t0038g0027 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.179-4169C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422631 | ||||||
chr17:81422649
|
C | G | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.179-4151C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422649 | ||||||
chr17:81423001
|
C | T | 1 | a0001c0025t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.179-3799C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423001 | ||||||
chr17:81423082
|
C | A | 2 | a0002c0001t0001g0157a0004c0004t0002g0158 | 2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.179-3718C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423082 | ||||||
chr17:81423087
|
C | A | 1 | a0003c0002t0001g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179-3713C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423087 | ||||||
chr17:81423214
|
T | G | 3 | a0001c0019t0003g0315a0005c0005t0005g0202a0005c0096t0005g0199 | 3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-3586T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423214 | ||||||
chr17:81423230
|
G | A | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.179-3570G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423230 | ||||||
chr17:81423263
|
C | T | 7 | a0001c0003t0003g0230a0002c0001t0001g0030a0002c0001t0001g0292others(4): Show | 7 | HG00609.hp1 HG02683.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-3537C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423263 | ||||||
chr17:81423366
|
A | G | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-3434A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423366 | ||||||
chr17:81423568
|
CCCCAGGT others(12): Show |
C | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-3225_179-3207d others(21): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81423568 | |||||
chr17:81423621
|
C | T | 1 | a0005c0066t0034g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.179-3179C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423621 | ||||||
chr17:81423650
|
T | TG | 5 | a0001c0009t0006g0134a0003c0002t0001g0096a0004c0004t0002g0266others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-3145dupG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81423650 | |||||
chr17:81423658
|
G | A | 2 | a0001c0003t0003g0083a0001c0010t0001g0082 | 2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.179-3142G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423658 | ||||||
chr17:81423668
|
A | G | 1 | a0001c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.179-3132A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423668 | ||||||
chr17:81423747
|
G | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-3053G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423747 | ||||||
chr17:81423755
|
T | C | 3 | a0001c0019t0003g0315a0005c0005t0005g0202a0005c0096t0005g0199 | 3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-3045T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423755 | ||||||
chr17:81423811
|
T | G | 97 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(94): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.179-2989T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423811 | ||||||
chr17:81423878
|
C | T | 32 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-2922C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423878 | ||||||
chr17:81423882
|
G | A | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-2918G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423882 | ||||||
chr17:81423950
|
G | A | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-2850G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423950 | ||||||
chr17:81423971
|
C | T | 31 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-2829C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423971 | ||||||
chr17:81423973
|
C | T | 3 | a0001c0019t0003g0315a0005c0005t0005g0202a0005c0096t0005g0199 | 3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-2827C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423973 | ||||||
chr17:81424003
|
A | G | 102 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(99): Show | 104 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.179-2797A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424003 | ||||||
chr17:81424031
|
G | A | 8 | a0001c0010t0004g0296a0001c0068t0008g0070a0003c0002t0001g0002others(5): Show | 9 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-2769G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424031 | ||||||
chr17:81424160
|
G | A | 4 | a0001c0007t0009g0260a0001c0007t0016g0234a0013c0097t0001g0235others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2640G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424160 | ||||||
chr17:81424260
|
C | T | 1 | a0018c0039t0011g0270 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.179-2540C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424260 | ||||||
chr17:81424489
|
T | G | 45 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(42): Show | 46 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.179-2311T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424489 | ||||||
chr17:81424646
|
G | A | 18 | a0001c0003t0003g0208a0001c0003t0003g0293a0001c0003t0003g0300others(15): Show | 19 | HG00408.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.179-2154G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424646 | ||||||
chr17:81424784
|
G | A | 3 | a0002c0001t0001g0281a0002c0001t0001g0282a0002c0055t0005g0283 | 3 | HG02027.hp1 HG02071.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.179-2016G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424784 | ||||||
chr17:81424884
|
TGTG | T | 3 | a0001c0019t0003g0315a0005c0005t0005g0202a0005c0096t0005g0199 | 3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-1913_179-1911d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81424884 | |||||
chr17:81424906
|
G | T | 4 | a0003c0002t0001g0039a0003c0002t0001g0095a0003c0002t0001g0096others(1): Show | 4 | NA18948.hp1 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-1894G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424906 | ||||||
chr17:81424917
|
G | A | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-1883G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424917 | ||||||
chr17:81424937
|
G | T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-1863G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424937 | ||||||
chr17:81424960
|
G | T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-1840G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424960 | ||||||
chr17:81424966
|
TGTG | T | 3 | a0001c0003t0003g0304a0001c0010t0001g0255a0002c0001t0001g0278 | 3 | HG00544.hp1 NA18975.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.179-1831_179-1829d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81424966 | |||||
chr17:81424970
|
G | T | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1830G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424970 | ||||||
chr17:81424972
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1828T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424972 | ||||||
chr17:81424989
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1811T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424989 | ||||||
chr17:81425045
|
GGGTGATG others(8): Show |
G | 1 | a0002c0016t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.179-1737_179-1723d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425045 | |||||
chr17:81425117
|
G | A | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1683G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425117 | ||||||
chr17:81425143
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1657T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425143 | ||||||
chr17:81425150
|
T | G | 41 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(38): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-1650T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425150 | ||||||
chr17:81425162
|
T | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-1638T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425162 | ||||||
chr17:81425164
|
G | T | 1 | a0004c0004t0014g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.179-1636G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425164 | ||||||
chr17:81425170
|
G | A | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1630G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425170 | ||||||
chr17:81425171
|
G | C | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1629G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425171 | ||||||
chr17:81425172
|
T | A | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1628T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425172 | ||||||
chr17:81425172
|
T | G | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-1628T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425172 | ||||||
chr17:81425173
|
G | C | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1627G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425173 | ||||||
chr17:81425174
|
G | T | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1626G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425174 | ||||||
chr17:81425175
|
T | A | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1625T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425175 | ||||||
chr17:81425179
|
A | C | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1621A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425179 | ||||||
chr17:81425181
|
T | C | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1619T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425181 | ||||||
chr17:81425182
|
GGTGGGTG others(41): Show |
G | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1617_179-1570d others(50): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425182 | ||||||
chr17:81425202
|
A | G | 51 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(48): Show | 52 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.179-1598A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425202 | ||||||
chr17:81425205
|
A | ATAG | 3 | a0002c0001t0001g0276a0005c0005t0005g0202a0015c0014t0001g0243 | 3 | HG00639.hp1 HG02723.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.179-1594_179-1593i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425205 | |||||
chr17:81425207
|
G | A | 48 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(45): Show | 49 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.179-1593G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425207 | ||||||
chr17:81425209
|
T | TGCTGGGT others(36): Show |
40 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(37): Show | 41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.179-1590_179-1589i others(45): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | |||||
chr17:81425209
|
T | TGGGTGAT others(8): Show |
266 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.179-1590_179-1576d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | |||||
chr17:81425209
|
T | TGGGTGAT others(333): Show |
1 | a0001c0012t0002g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.179-1576_179-1575i others(342): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | |||||
chr17:81425209
|
T | TGGTGGGT others(36): Show |
8 | a0001c0007t0009g0014a0001c0007t0016g0161a0001c0019t0003g0315others(5): Show | 8 | HG02451.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-1589_179-1588i others(45): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | |||||
chr17:81425221
|
T | TTGGTGAT others(29): Show |
2 | a0002c0001t0001g0276a0015c0014t0001g0243 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.179-1574_179-1573i others(38): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425221 | |||||
chr17:81425225
|
T | G | 7 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1575T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425225 | ||||||
chr17:81425225
|
T | TGATGATG others(3): Show |
1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1574_179-1573i others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425225 | |||||
chr17:81425234
|
G | T | 1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1566G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425234 | ||||||
chr17:81425236
|
TTGGGGGT others(5): Show |
T | 7 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1560_179-1549d others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425236 | |||||
chr17:81425247
|
A | G | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1553A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425247 | ||||||
chr17:81425248
|
G | T | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1552G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425248 | ||||||
chr17:81425254
|
A | G | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1546A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425254 | ||||||
chr17:81425281
|
G | A | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1519G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425281 | ||||||
chr17:81425282
|
G | T | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1518G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425282 | ||||||
chr17:81425283
|
T | G | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1517T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425283 | ||||||
chr17:81425284
|
G | A | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1516G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425284 | ||||||
chr17:81425288
|
A | G | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1512A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425288 | ||||||
chr17:81425305
|
GTGGGTGA others(6): Show |
G | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1490_179-1478d others(15): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425305 | |||||
chr17:81425311
|
GA | G | 8 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-1488delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425311 | ||||||
chr17:81425316
|
G | A | 7 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1484G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425316 | ||||||
chr17:81425327
|
ATAG | A | 5 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-1471_179-1469d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425327 | |||||
chr17:81425350
|
T | G | 1 | a0004c0004t0002g0219 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.179-1450T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425350 | ||||||
chr17:81425390
|
TGGTGATA others(110): Show |
T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-1380_179-1264d others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425390 | |||||
chr17:81425398
|
GTGGTGGG others(9): Show |
G | 1 | a0001c0003t0003g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.179-1379_179-1364d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425398 | |||||
chr17:81425404
|
G | GGTGATGT others(7): Show |
88 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(85): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.179-1394_179-1381d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425404 | |||||
chr17:81425409
|
T | TGTGGGTG others(6): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1387_179-1386i others(15): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425409 | |||||
chr17:81425418
|
TGG | T | 8 | a0001c0007t0009g0014a0001c0007t0016g0161a0001c0019t0003g0315others(5): Show | 8 | HG02630.hp2 HG02965.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-1380_179-1379d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425418 | |||||
chr17:81425419
|
GGGTGATG others(8): Show |
G | 1 | a0004c0011t0023g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.179-1366_179-1352d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425419 | |||||
chr17:81425434
|
T | TG | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1364dupG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425434 | |||||
chr17:81425436
|
GTGATGTG others(34): Show |
G | 2 | a0001c0007t0009g0014a0001c0007t0016g0161 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.179-1363_179-1323d others(43): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425436 | ||||||
chr17:81425444
|
G | C | 2 | a0013c0027t0001g0025a0013c0027t0001g0026 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-1356G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425444 | ||||||
chr17:81425446
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1354T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425446 | ||||||
chr17:81425449
|
G | T | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1351G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425449 | ||||||
chr17:81425455
|
TA | T | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1344delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425455 | ||||||
chr17:81425461
|
T | TTGG | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1339_179-1338i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425461 | ||||||
chr17:81425463
|
GGTGATGT others(7): Show |
G | 29 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-1321_179-1308d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425463 | |||||
chr17:81425468
|
T | TA | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1332_179-1331i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425468 | ||||||
chr17:81425473
|
TTG | T | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1326_179-1325d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425473 | ||||||
chr17:81425477
|
T | G | 6 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(3): Show | 6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1323T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425477 | ||||||
chr17:81425477
|
TGTGATGT others(9): Show |
T | 40 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(37): Show | 41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.179-1309_179-1294d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425477 | |||||
chr17:81425481
|
A | G | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-1319A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425481 | ||||||
chr17:81425491
|
TGG | T | 5 | a0001c0019t0003g0315a0001c0026t0003g0246a0005c0005t0005g0202others(2): Show | 5 | HG02965.hp2 NA18963.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-1307_179-1306d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425491 | |||||
chr17:81425531
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1269T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425531 | ||||||
chr17:81425556
|
T | C | 1 | a0002c0001t0001g0084 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.179-1244T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425556 | ||||||
chr17:81425565
|
TGGTGATG others(21): Show |
T | 1 | a0008c0073t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.179-1192_179-1165d others(30): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425565 | |||||
chr17:81425616
|
G | C | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-1184G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425616 | ||||||
chr17:81425625
|
GATGTGGT others(8): Show |
G | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-1160_179-1146d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425625 | |||||
chr17:81425640
|
T | G | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1160T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425640 | ||||||
chr17:81425640
|
TATGTGGT others(8): Show |
T | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-1141_179-1127d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425640 | |||||
chr17:81425687
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1113T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425687 | ||||||
chr17:81425711
|
ATAG | A | 41 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(38): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-1087_179-1085d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425711 | |||||
chr17:81425735
|
GGTGATGT others(7): Show |
G | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1049_179-1036d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425735 | |||||
chr17:81425759
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1041T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425759 | ||||||
chr17:81425765
|
GTGATGTG others(8): Show |
G | 2 | a0013c0027t0001g0025a0013c0027t0001g0026 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-1023_179-1009d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425765 | |||||
chr17:81425770
|
G | C | 7 | a0001c0094t0009g0016a0002c0001t0002g0132a0004c0011t0002g0023others(4): Show | 7 | HG02895.hp2 HG03017.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1030G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425770 | ||||||
chr17:81425812
|
T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-988T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425812 | ||||||
chr17:81425882
|
TGGTGATG others(9): Show |
T | 2 | a0013c0027t0001g0025a0013c0027t0001g0026 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-909_179-894del others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425882 | |||||
chr17:81425905
|
G | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-895G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425905 | ||||||
chr17:81425907
|
C | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-893C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425907 | ||||||
chr17:81425908
|
A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-892A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425908 | ||||||
chr17:81425910
|
T | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-890T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425910 | ||||||
chr17:81425921
|
T | TTGGGGGT others(5): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-876_179-875ins others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425921 | |||||
chr17:81425927
|
C | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-873C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425927 | ||||||
chr17:81425928
|
A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-872A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425928 | ||||||
chr17:81425936
|
A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-864A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425936 | ||||||
chr17:81425955
|
G | A | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-845G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425955 | ||||||
chr17:81425993
|
T | TGGTGATA others(34): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-806_179-805ins others(41): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425993 | |||||
chr17:81425995
|
A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-805A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425995 | ||||||
chr17:81426000
|
G | T | 41 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(38): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-800G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426000 | ||||||
chr17:81426016
|
G | A | 1 | a0001c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.179-784G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426016 | ||||||
chr17:81426033
|
T | TGGTGATA others(6): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-761_179-760ins others(13): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426033 | |||||
chr17:81426044
|
C | T | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-756C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426044 | ||||||
chr17:81426046
|
C | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-754C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426046 | ||||||
chr17:81426048
|
T | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-752T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426048 | ||||||
chr17:81426053
|
G | A | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-747G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426053 | ||||||
chr17:81426055
|
G | A | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-745G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426055 | ||||||
chr17:81426055
|
G | GGGGGGGG others(761): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-744_179-743ins others(768): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | |||||
chr17:81426055
|
G | GGTGGTGG others(811): Show |
29 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(818): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | |||||
chr17:81426055
|
G | GGTGGTGG others(1771): Show |
1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1778): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | |||||
chr17:81426055
|
G | GGTGGTGG others(811): Show |
1 | a0030c0090t0002g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(818): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | |||||
chr17:81426075
|
G | GGGGTGAT others(6): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-725_179-724ins others(13): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426075 | ||||||
chr17:81426076
|
T | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-724T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426076 | ||||||
chr17:81426076
|
T | TGATGATG others(796): Show |
1 | a0002c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-723_179-722ins others(803): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATA others(1698): Show |
1 | a0002c0001t0001g0004 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.179-718_179-717ins others(1705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(796): Show |
1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(803): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4000): Show |
3 | a0007c0008t0001g0005a0007c0008t0001g0021a0015c0014t0001g0001 | 4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1713): Show |
1 | a0001c0003t0003g0314 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2321): Show |
1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2328): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4081): Show |
1 | a0001c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(4088): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(545): Show |
4 | a0018c0106t0010g0328a0019c0105t0001g0249a0025c0107t0002g0250others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(552): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1688): Show |
1 | a0004c0011t0023g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1695): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(471): Show |
38 | a0001c0010t0004g0121a0001c0025t0003g0065a0001c0025t0003g0212others(35): Show | 38 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(478): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1698): Show |
1 | a0003c0002t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1713): Show |
1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(796): Show |
6 | a0002c0001t0001g0320a0003c0018t0001g0307a0014c0022t0011g0322others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(803): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1712): Show |
1 | a0002c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1719): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1670): Show |
1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1677): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2182): Show |
1 | a0002c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2189): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1715): Show |
1 | a0001c0003t0003g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1722): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1713): Show |
147 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(144): Show | 148 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2182): Show |
5 | a0001c0009t0006g0134a0002c0081t0001g0043a0004c0004t0002g0061others(2): Show | 5 | HG01261.hp1 HG01928.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(2189): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1712): Show |
1 | a0023c0084t0003g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1719): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1710): Show |
4 | a0002c0001t0006g0148a0002c0001t0007g0147a0002c0062t0007g0152others(1): Show | 4 | HG00738.hp1 HG02300.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(1717): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1685): Show |
2 | a0001c0032t0003g0232a0034c0033t0001g0178 | 2 | HG01981.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.179-702_179-701ins others(1692): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1711): Show |
1 | a0003c0002t0004g0171 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1718): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1712): Show |
1 | a0045c0080t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1719): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1713): Show |
1 | a0029c0070t0003g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1713): Show |
1 | a0006c0006t0001g0151 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1713): Show |
1 | a0002c0001t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1698): Show |
1 | a0001c0012t0002g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(6192): Show |
1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(6199): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2306): Show |
4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(2313): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2981): Show |
1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2988): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(5562): Show |
1 | a0013c0027t0001g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(5569): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(5478): Show |
1 | a0013c0027t0001g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(5485): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(471): Show |
1 | a0002c0044t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(478): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3629): Show |
1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3636): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2704): Show |
1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(2711): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(5055): Show |
1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(5062): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3321): Show |
1 | a0001c0019t0003g0315 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(3328): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3533): Show |
1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3540): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3321): Show |
1 | a0005c0096t0005g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3328): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1898): Show |
2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-702_179-701ins others(1905): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4000): Show |
1 | a0007c0048t0002g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4000): Show |
4 | a0003c0002t0004g0310a0007c0008t0001g0309a0007c0008t0001g0312others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3071): Show |
1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3078): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1756): Show |
1 | a0005c0028t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1763): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2701): Show |
1 | a0008c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(2708): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4000): Show |
1 | a0004c0037t0014g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4185): Show |
4 | a0001c0003t0003g0110a0001c0003t0003g0302a0002c0001t0001g0321others(1): Show | 4 | HG02132.hp1 NA18947.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4192): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4000): Show |
1 | a0005c0005t0012g0204 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4000): Show |
15 | a0001c0010t0001g0034a0001c0012t0002g0112a0001c0026t0003g0247others(12): Show | 15 | HG01074.hp2 HG02165.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3997): Show |
4 | a0003c0002t0001g0124a0003c0002t0001g0213a0003c0002t0004g0122others(1): Show | 4 | HG00423.hp2 HG00544.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4004): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4241): Show |
1 | a0039c0058t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(4248): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3959): Show |
1 | a0001c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3966): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(3999): Show |
1 | a0001c0007t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4006): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2516): Show |
1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2523): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(1534): Show |
1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1541): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(4004): Show |
1 | a0001c0009t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4011): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426076
|
T | TGGTGATG others(2698): Show |
1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(2705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | |||||
chr17:81426081
|
A | ATGTGGTT others(1713): Show |
1 | a0002c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426081 | |||||
chr17:81426091
|
T | TGGTGATA others(1685): Show |
2 | a0001c0003t0003g0286a0001c0003t0003g0290 | 2 | NA18963.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.179-702_179-701ins others(1692): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426091 | |||||
chr17:81426099
|
G | A | 5 | a0001c0003t0003g0289a0001c0007t0009g0260a0001c0007t0016g0234others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-701G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426099 | ||||||
chr17:81426101
|
G | T | 5 | a0001c0003t0003g0289a0001c0007t0009g0260a0001c0007t0016g0234others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-699G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426101 | ||||||
chr17:81426105
|
G | A | 4 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-695G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426105 | ||||||
chr17:81426106
|
G | T | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-694G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426106 | ||||||
chr17:81426119
|
T | G | 5 | a0001c0003t0003g0289a0001c0007t0009g0260a0001c0007t0016g0234others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-681T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426119 | ||||||
chr17:81426125
|
TA | T | 322 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(319): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.179-674delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426125 | ||||||
chr17:81426126
|
A | AGTGGTGG others(2432): Show |
1 | a0017c0023t0015g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179-669_179-668ins others(2439): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | |||||
chr17:81426126
|
A | AGTGGTGG others(2431): Show |
1 | a0001c0007t0009g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.179-669_179-668ins others(2438): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | |||||
chr17:81426126
|
A | AGTGGTGG others(2548): Show |
1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-669_179-668ins others(2555): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | |||||
chr17:81426126
|
A | AGTGGTGG others(2221): Show |
1 | a0001c0007t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.179-669_179-668ins others(2228): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | |||||
chr17:81426131
|
T | TGGGTGAT others(1682): Show |
1 | a0001c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.179-669_179-668ins others(1689): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426131 | ||||||
chr17:81426152
|
G | A | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-648G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426152 | ||||||
chr17:81426180
|
A | G | 39 | a0001c0010t0004g0121a0001c0025t0003g0065a0001c0025t0003g0212others(36): Show | 39 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.179-620A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426180 | ||||||
chr17:81426208
|
A | ATGATGTG others(437): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-548_179-547ins others(444): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426208 | |||||
chr17:81426208
|
A | ATGATGTG others(438): Show |
30 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.179-548_179-547ins others(445): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426208 | |||||
chr17:81426253
|
A | G | 48 | a0001c0010t0004g0121a0001c0010t0004g0296a0001c0019t0003g0315others(45): Show | 49 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.179-547A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426253 | ||||||
chr17:81426284
|
T | A | 44 | a0001c0007t0009g0260a0001c0007t0016g0234a0001c0010t0004g0121others(41): Show | 44 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-516T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426284 | ||||||
chr17:81426284
|
TGTG | T | 5 | a0001c0010t0009g0185a0010c0031t0004g0018a0010c0102t0004g0017others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-511_179-509del others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426284 | |||||
chr17:81426309
|
G | T | 31 | a0001c0009t0025g0252a0001c0009t0037g0319a0001c0012t0002g0137others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-491G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426309 | ||||||
chr17:81426333
|
T | TGGTGATA others(49): Show |
38 | a0001c0010t0004g0121a0001c0025t0003g0065a0001c0025t0003g0212others(35): Show | 38 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.179-412_179-411ins others(56): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426333 | |||||
chr17:81426342
|
T | C | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-458T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426342 | ||||||
chr17:81426344
|
G | T | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-456G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426344 | ||||||
chr17:81426371
|
G | GGTGGGTG others(221): Show |
1 | a0002c0044t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-412_179-411ins others(228): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426371 | |||||
chr17:81426389
|
T | G | 1 | a0002c0044t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-411T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426389 | ||||||
chr17:81426399
|
C | G | 1 | a0002c0044t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-401C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426399 | ||||||
chr17:81426445
|
G | T | 1 | a0002c0044t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-355G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426445 | ||||||
chr17:81426447
|
G | T | 4 | a0001c0007t0009g0260a0001c0007t0016g0234a0013c0097t0001g0235others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-353G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426447 | ||||||
chr17:81426451
|
T | TAGCG | 4 | a0018c0106t0010g0328a0019c0105t0001g0249a0025c0107t0002g0250others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-349_179-348ins others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | ||||||
chr17:81426451
|
T | TAGTCGTG others(5514): Show |
1 | a0002c0044t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-349_179-348ins others(5521): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | ||||||
chr17:81426451
|
T | TAGTG | 94 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0003g0302others(91): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.179-349_179-348ins others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | ||||||
chr17:81426451
|
T | TAGTGGTG others(262): Show |
2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-349_179-348ins others(269): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | ||||||
chr17:81426451
|
T | TAGTGGTG others(832): Show |
1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-349_179-348ins others(839): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | ||||||
chr17:81426489
|
A | G | 1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-311A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426489 | ||||||
chr17:81426493
|
C | T | 1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-307C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426493 | ||||||
chr17:81426495
|
C | G | 1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-305C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426495 | ||||||
chr17:81426511
|
G | A | 1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-289G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426511 | ||||||
chr17:81426515
|
T | TGTGGTTG others(1565): Show |
1 | a0001c0051t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-282_179-281ins others(1572): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426515 | |||||
chr17:81426682
|
T | C | 185 | a0001c0003t0003g0048a0001c0003t0003g0053a0001c0003t0003g0068others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.179-118T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426682 | ||||||
chr17:81426683
|
G | C | 1 | a0005c0005t0012g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.179-117G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426683 | ||||||
chr17:81427077
|
G | A | 3 | a0001c0012t0002g0058a0001c0012t0002g0159a0011c0015t0001g0166 | 3 | HG01346.hp2 HG02451.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.358+98G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427077 | ||||||
chr17:81427089
|
C | T | 2 | a0003c0064t0005g0198a0032c0071t0003g0006 | 2 | NA18966.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.358+110C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427089 | ||||||
chr17:81427115
|
G | A | 2 | a0002c0001t0001g0276a0015c0014t0001g0243 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.358+136G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427115 | ||||||
chr17:81427156
|
G | A | 5 | a0001c0012t0002g0112a0005c0005t0012g0204a0005c0005t0012g0206others(2): Show | 5 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+177G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427156 | ||||||
chr17:81427173
|
A | G | 1 | a0003c0002t0001g0106 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.358+194A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427173 | ||||||
chr17:81427186
|
C | T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358+207C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427186 | ||||||
chr17:81427236
|
CAG | C | 4 | a0001c0010t0009g0185a0001c0094t0009g0016a0010c0031t0004g0015others(1): Show | 4 | HG02622.hp1 HG02895.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+258_358+259del others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427236 | ||||||
chr17:81427365
|
C | G | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+386C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427365 | ||||||
chr17:81427489
|
A | G | 108 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0003t0010g0211others(105): Show | 109 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.358+510A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427489 | ||||||
chr17:81427507
|
G | A | 4 | a0001c0003t0003g0314a0001c0094t0009g0016a0010c0031t0004g0015others(1): Show | 4 | HG02895.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+528G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427507 | ||||||
chr17:81427553
|
G | A | 1 | a0002c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.358+574G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427553 | ||||||
chr17:81427651
|
C | T | 1 | a0003c0002t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.358+672C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427651 | ||||||
chr17:81427697
|
A | C | 3 | a0005c0005t0012g0204a0005c0005t0012g0206a0005c0005t0012g0207 | 3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.358+718A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427697 | ||||||
chr17:81427708
|
G | A | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.358+729G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427708 | ||||||
chr17:81427749
|
G | A | 4 | a0001c0003t0003g0067a0004c0004t0002g0167a0004c0004t0002g0240others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+770G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427749 | ||||||
chr17:81427858
|
C | T | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.358+879C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427858 | ||||||
chr17:81427860
|
C | T | 1 | a0002c0001t0006g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.358+881C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427860 | ||||||
chr17:81427864
|
G | A | 8 | a0001c0094t0009g0016a0002c0001t0001g0242a0002c0001t0002g0132others(5): Show | 8 | HG02280.hp1 HG02698.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+885G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427864 | ||||||
chr17:81427881
|
C | T | 3 | a0002c0001t0001g0276a0003c0002t0013g0024a0015c0014t0001g0243 | 3 | HG00639.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.358+902C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427881 | ||||||
chr17:81427889
|
C | T | 38 | a0001c0003t0003g0053a0001c0003t0003g0110a0001c0007t0033g0135others(35): Show | 39 | HG00423.hp2 HG00544.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.358+910C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427889 | ||||||
chr17:81427953
|
A | G | 15 | a0001c0003t0003g0110a0001c0012t0002g0112a0001c0051t0001g0288others(12): Show | 15 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.358+974A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427953 | ||||||
chr17:81428175
|
C | T | 125 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(122): Show | 125 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.358+1196C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428175 | ||||||
chr17:81428241
|
G | A | 2 | a0002c0001t0001g0276a0015c0014t0001g0243 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.358+1262G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428241 | ||||||
chr17:81428306
|
A | C | 7 | a0001c0003t0003g0068a0001c0003t0003g0231a0001c0003t0003g0233others(4): Show | 7 | HG00323.hp1 HG00639.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1327A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428306 | ||||||
chr17:81428362
|
C | T | 1 | a0001c0069t0007g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.358+1383C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428362 | ||||||
chr17:81428484
|
G | A | 2 | a0002c0001t0001g0276a0015c0014t0001g0243 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.358+1505G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428484 | ||||||
chr17:81428522
|
C | T | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.358+1543C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428522 | ||||||
chr17:81428534
|
C | G | 22 | a0001c0069t0007g0253a0001c0094t0009g0016a0001c0103t0026g0245others(19): Show | 23 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+1555C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428534 | ||||||
chr17:81428552
|
C | G | 7 | a0001c0009t0024g0248a0001c0009t0025g0252a0001c0010t0009g0185others(4): Show | 7 | HG01261.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1573C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428552 | ||||||
chr17:81428661
|
C | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+1682C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428661 | ||||||
chr17:81428762
|
C | T | 2 | a0001c0086t0003g0031a0002c0044t0001g0164 | 2 | HG00609.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.358+1783C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428762 | ||||||
chr17:81428830
|
C | T | 9 | a0001c0069t0007g0253a0001c0094t0009g0016a0002c0001t0002g0132others(6): Show | 9 | HG02451.hp1 HG02895.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+1851C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428830 | ||||||
chr17:81428858
|
C | T | 16 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(13): Show | 17 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+1879C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428858 | ||||||
chr17:81428896
|
A | G | 18 | a0001c0007t0009g0014a0001c0007t0016g0161a0001c0007t0033g0135others(15): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+1917A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428896 | ||||||
chr17:81428915
|
G | A | 7 | a0001c0101t0010g0020a0002c0001t0001g0274a0002c0001t0001g0324others(4): Show | 7 | HG01074.hp2 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1936G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428915 | ||||||
chr17:81429125
|
T | G | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+2146T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429125 | ||||||
chr17:81429165
|
C | T | 1 | a0001c0025t0003g0065 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.358+2186C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429165 | ||||||
chr17:81429187
|
A | G | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+2208A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429187 | ||||||
chr17:81429188
|
G | T | 18 | a0001c0007t0009g0260a0001c0007t0016g0234a0001c0009t0037g0319others(15): Show | 19 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+2209G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429188 | ||||||
chr17:81429310
|
C | G | 7 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+2331C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429310 | ||||||
chr17:81429338
|
C | G | 2 | a0001c0003t0003g0053a0034c0033t0001g0178 | 2 | HG02523.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.358+2359C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429338 | ||||||
chr17:81429446
|
C | T | 1 | a0002c0056t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.358+2467C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429446 | ||||||
chr17:81429477
|
G | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+2498G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429477 | ||||||
chr17:81429518
|
T | A | 1 | a0008c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.358+2539T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429518 | ||||||
chr17:81429551
|
G | A | 1 | a0001c0007t0002g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.358+2572G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429551 | ||||||
chr17:81429552
|
C | A | 1 | a0003c0002t0013g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358+2573C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429552 | ||||||
chr17:81429751
|
A | AC | 5 | a0001c0025t0003g0065a0002c0001t0002g0130a0002c0016t0001g0052others(2): Show | 5 | HG01433.hp1 HG02135.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+2777dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81429751 | |||||
chr17:81429751
|
A | G | 1 | a0001c0012t0002g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.358+2772A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429751 | ||||||
chr17:81429855
|
C | T | 3 | a0001c0007t0009g0014a0001c0007t0016g0161a0047c0046t0004g0273 | 3 | HG02630.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.358+2876C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429855 | ||||||
chr17:81429857
|
G | T | 7 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+2878G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429857 | ||||||
chr17:81429973
|
G | A | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.358+2994G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429973 | ||||||
chr17:81429983
|
G | A | 1 | a0030c0090t0002g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.358+3004G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429983 | ||||||
chr17:81430002
|
G | A | 1 | a0025c0107t0002g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.358+3023G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430002 | ||||||
chr17:81430022
|
C | A | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.358+3043C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430022 | ||||||
chr17:81430027
|
T | C | 46 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0016g0234others(43): Show | 47 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+3048T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430027 | ||||||
chr17:81430030
|
C | A | 16 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(13): Show | 17 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+3051C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430030 | ||||||
chr17:81430219
|
C | G | 1 | a0001c0003t0003g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.358+3240C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430219 | ||||||
chr17:81430341
|
C | T | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.358+3362C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430341 | ||||||
chr17:81430394
|
G | A | 9 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0012t0002g0133others(6): Show | 9 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+3415G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430394 | ||||||
chr17:81430408
|
C | T | 4 | a0001c0007t0009g0260a0001c0007t0016g0161a0017c0023t0015g0277others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+3429C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430408 | ||||||
chr17:81430552
|
C | T | 4 | a0004c0037t0014g0256a0018c0106t0010g0328a0019c0105t0001g0249others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3573C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430552 | ||||||
chr17:81430656
|
C | T | 1 | a0008c0073t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.358+3677C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430656 | ||||||
chr17:81430668
|
C | T | 12 | a0001c0003t0003g0186a0004c0004t0002g0092a0004c0004t0002g0093others(9): Show | 12 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.358+3689C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430668 | ||||||
chr17:81430716
|
T | C | 1 | a0001c0085t0001g0073 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.358+3737T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430716 | ||||||
chr17:81430763
|
C | T | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+3784C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430763 | ||||||
chr17:81430802
|
G | A | 4 | a0004c0037t0014g0256a0018c0106t0010g0328a0025c0107t0002g0250others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3823G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430802 | ||||||
chr17:81430839
|
C | T | 21 | a0001c0009t0037g0319a0003c0018t0002g0143a0004c0004t0002g0003others(18): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.358+3860C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430839 | ||||||
chr17:81430965
|
G | A | 29 | a0001c0007t0009g0260a0001c0007t0016g0234a0001c0009t0037g0319others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.358+3986G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430965 | ||||||
chr17:81430984
|
CCGGCGTG others(27): Show |
C | 10 | a0001c0007t0015g0275a0001c0101t0010g0020a0002c0001t0001g0274others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+4039_358+4072d others(36): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81430984 | |||||
chr17:81431018
|
TCGGCGTG others(27): Show |
T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+4070_358+4103d others(36): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81431018 | |||||
chr17:81431090
|
C | T | 1 | a0008c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.358+4111C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431090 | ||||||
chr17:81431091
|
G | A | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+4112G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431091 | ||||||
chr17:81431097
|
G | A | 9 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0012t0002g0133others(6): Show | 9 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+4118G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431097 | ||||||
chr17:81431118
|
G | A | 2 | a0005c0005t0005g0202a0005c0096t0005g0199 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.358+4139G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431118 | ||||||
chr17:81431185
|
C | T | 1 | a0004c0004t0002g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358+4206C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431185 | ||||||
chr17:81431186
|
G | A | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+4207G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431186 | ||||||
chr17:81431265
|
T | TGCCA | 4 | a0002c0001t0001g0320a0014c0022t0011g0322a0014c0022t0011g0323others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4288_358+4291d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81431265 | |||||
chr17:81431271
|
G | C | 28 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0033g0135others(25): Show | 29 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.358+4292G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431271 | ||||||
chr17:81431283
|
C | T | 8 | a0001c0069t0007g0253a0001c0094t0009g0016a0002c0001t0002g0132others(5): Show | 8 | HG02451.hp1 HG02895.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+4304C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431283 | ||||||
chr17:81431324
|
A | G | 132 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.358+4345A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431324 | ||||||
chr17:81431325
|
A | G | 4 | a0003c0002t0001g0039a0003c0002t0001g0095a0003c0002t0001g0096others(1): Show | 4 | NA18948.hp1 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4346A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431325 | ||||||
chr17:81431349
|
GCAT | G | 72 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0009g0014others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.358+4371_358+4373d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431349 | ||||||
chr17:81431545
|
T | C | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.358+4566T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431545 | ||||||
chr17:81431560
|
C | A | 1 | a0001c0021t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.358+4581C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431560 | ||||||
chr17:81431607
|
A | C | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+4628A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431607 | ||||||
chr17:81431623
|
T | G | 25 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0033g0135others(22): Show | 26 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+4644T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431623 | ||||||
chr17:81431702
|
C | T | 2 | a0001c0007t0009g0014a0001c0007t0016g0161 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.358+4723C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431702 | ||||||
chr17:81431719
|
C | T | 2 | a0018c0106t0010g0328a0019c0105t0001g0249 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.358+4740C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431719 | ||||||
chr17:81431777
|
C | G | 31 | a0001c0007t0009g0260a0001c0007t0016g0234a0001c0009t0037g0319others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.358+4798C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431777 | ||||||
chr17:81431801
|
G | C | 28 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0033g0135others(25): Show | 29 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.358+4822G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431801 | ||||||
chr17:81431837
|
C | T | 1 | a0001c0025t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.358+4858C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431837 | ||||||
chr17:81431931
|
G | A | 11 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+4952G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431931 | ||||||
chr17:81431968
|
C | T | 25 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0033g0135others(22): Show | 26 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+4989C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431968 | ||||||
chr17:81431975
|
G | A | 4 | a0001c0003t0003g0067a0001c0003t0003g0186a0002c0001t0001g0131others(1): Show | 4 | HG01361.hp1 HG01515.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4996G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431975 | ||||||
chr17:81432210
|
G | A | 1 | a0004c0004t0002g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.358+5231G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432210 | ||||||
chr17:81432260
|
G | A | 2 | a0002c0001t0001g0136a0003c0002t0004g0205 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.358+5281G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432260 | ||||||
chr17:81432357
|
G | A | 1 | a0001c0007t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.358+5378G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432357 | ||||||
chr17:81432477
|
G | A | 2 | a0001c0007t0009g0014a0001c0007t0016g0161 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.358+5498G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432477 | ||||||
chr17:81432481
|
ACTGTCCA others(28): Show |
A | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.358+5503_358+5537d others(37): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432481 | ||||||
chr17:81432508
|
G | A | 1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.358+5529G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432508 | ||||||
chr17:81432544
|
A | ATCAGGCC others(17): Show |
15 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(12): Show | 16 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.358+5565_358+5566i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432544 | ||||||
chr17:81432545
|
C | T | 1 | a0003c0002t0013g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358+5566C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432545 | ||||||
chr17:81432547
|
A | AGGCCCAC others(17): Show |
55 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0009g0014others(52): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.358+5582_358+5605d others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432547 | |||||
chr17:81432547
|
A | AGGCCCAC others(42): Show |
1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+5597_358+5598i others(51): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432547 | |||||
chr17:81432547
|
A | G | 15 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(12): Show | 16 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.358+5568A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432547 | ||||||
chr17:81432557
|
T | TCCCTCCC others(37): Show |
15 | a0001c0003t0003g0047a0001c0003t0003g0053a0001c0007t0015g0275others(12): Show | 15 | HG01361.hp1 HG02155.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.358+5605_358+5606i others(46): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | |||||
chr17:81432557
|
T | TCCCTCCC others(61): Show |
26 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0050others(23): Show | 26 | HG00639.hp1 HG00673.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+5605_358+5606i others(70): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | |||||
chr17:81432557
|
T | TCCCTCCC others(105): Show |
1 | a0002c0063t0020g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.358+5605_358+5606i others(114): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | |||||
chr17:81432557
|
T | TCCCTCCC others(85): Show |
3 | a0010c0031t0004g0018a0010c0102t0004g0017a0019c0036t0001g0019 | 3 | HG02258.hp2 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.358+5605_358+5606i others(94): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | |||||
chr17:81432557
|
T | TCCCTCCC others(62): Show |
1 | a0001c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.358+5605_358+5606i others(71): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | |||||
chr17:81432570
|
C | CGGGCCCA others(17): Show |
2 | a0005c0005t0005g0202a0005c0096t0005g0199 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.358+5605_358+5606i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432570 | |||||
chr17:81432697
|
G | GCATCCCC others(41): Show |
1 | a0001c0003t0003g0300 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.359-5651_359-5650i others(50): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432697 | |||||
chr17:81432697
|
G | GCATCCCC others(17): Show |
1 | a0005c0066t0034g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.359-5652_359-5651i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432697 | |||||
chr17:81432720
|
G | C | 2 | a0001c0003t0003g0300a0005c0066t0034g0313 | 2 | HG03942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.359-5650G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432720 | ||||||
chr17:81432720
|
G | GCCATCCC others(17): Show |
298 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(295): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.359-5640_359-5639i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432720 | |||||
chr17:81432720
|
G | GCCATCCC others(18): Show |
4 | a0003c0002t0001g0104a0003c0002t0001g0105a0003c0002t0001g0213others(1): Show | 4 | HG01928.hp1 HG02080.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-5640_359-5639i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432720 | |||||
chr17:81432720
|
G | GCCATCCC others(17): Show |
2 | a0002c0016t0001g0052a0002c0052t0001g0045 | 2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.359-5640_359-5639i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432720 | |||||
chr17:81432729
|
A | AGGCCCAC others(18): Show |
1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-5640_359-5639i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432729 | |||||
chr17:81432731
|
A | G | 16 | a0001c0003t0003g0286a0001c0003t0003g0289a0001c0007t0009g0014others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.359-5639A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432731 | ||||||
chr17:81432736
|
C | CCCTCCCC others(16): Show |
1 | a0001c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.359-5625_359-5624i others(25): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432736 | |||||
chr17:81432743
|
CCCGAGCC others(17): Show |
C | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5624_359-5601d others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432743 | |||||
chr17:81432746
|
G | C | 13 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-5624G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432746 | ||||||
chr17:81432748
|
G | T | 13 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-5622G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432748 | ||||||
chr17:81432766
|
C | CCCCGAGC others(66): Show |
7 | a0002c0001t0001g0169a0002c0001t0001g0174a0003c0002t0004g0170others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-5604_359-5603i others(75): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432766 | ||||||
chr17:81432767
|
T | C | 13 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-5603T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432767 | ||||||
chr17:81432770
|
C | G | 5 | a0001c0007t0009g0014a0001c0007t0016g0161a0003c0002t0013g0024others(2): Show | 5 | HG02630.hp2 HG03486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-5600C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432770 | ||||||
chr17:81432772
|
T | G | 6 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(3): Show | 6 | HG02630.hp2 HG03486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-5598T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432772 | ||||||
chr17:81432779
|
G | A | 7 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(4): Show | 7 | HG02630.hp2 HG02976.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-5591G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432779 | ||||||
chr17:81432791
|
C | T | 6 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(3): Show | 6 | HG02630.hp2 HG03486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-5579C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432791 | ||||||
chr17:81432793
|
CA | C | 8 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0016g0161others(5): Show | 8 | HG02630.hp2 HG02976.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-5576delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432793 | ||||||
chr17:81432795
|
C | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5575C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432795 | ||||||
chr17:81432797
|
T | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5573T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432797 | ||||||
chr17:81432804
|
G | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5566G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432804 | ||||||
chr17:81432815
|
G | C | 37 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5555G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432815 | ||||||
chr17:81432815
|
G | GCCCCATC others(65): Show |
11 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-5543_359-5542i others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432815 | |||||
chr17:81432815
|
G | GCCCCATC others(18): Show |
1 | a0002c0001t0002g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.359-5533_359-5509d others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432815 | |||||
chr17:81432818
|
C | CA | 37 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5552_359-5551i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432818 | ||||||
chr17:81432833
|
C | CCCTCCCC others(42): Show |
2 | a0001c0012t0002g0112a0039c0058t0017g0191 | 2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.359-5492_359-5444d others(51): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432833 | |||||
chr17:81432836
|
TC | T | 37 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5526delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432836 | |||||
chr17:81432840
|
C | G | 37 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5530C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432840 | ||||||
chr17:81432842
|
C | T | 1 | a0002c0056t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.359-5528C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432842 | ||||||
chr17:81432843
|
C | A | 11 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-5527C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432843 | ||||||
chr17:81432857
|
A | C | 9 | a0001c0007t0015g0275a0001c0101t0010g0020a0002c0001t0001g0274others(6): Show | 9 | HG01074.hp2 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-5513A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432857 | ||||||
chr17:81432861
|
T | TC | 43 | a0001c0007t0009g0014a0001c0007t0009g0260a0001c0007t0016g0161others(40): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.359-5509_359-5508i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432861 | ||||||
chr17:81432862
|
T | C | 56 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.359-5508T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432862 | ||||||
chr17:81432864
|
C | G | 11 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-5506C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432864 | ||||||
chr17:81432872
|
C | T | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.359-5498C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432872 | ||||||
chr17:81432882
|
A | C | 53 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.359-5488A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432882 | ||||||
chr17:81432885
|
TC | T | 42 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5477delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432885 | |||||
chr17:81432887
|
C | T | 42 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5483C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432887 | ||||||
chr17:81432887
|
CCCCCCCA others(17): Show |
C | 76 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(73): Show | 77 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.359-5467_359-5444d others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432887 | |||||
chr17:81432888
|
CCCCCCAT others(16): Show |
C | 1 | a0009c0013t0006g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.359-5476_359-5454d others(25): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432888 | |||||
chr17:81432891
|
C | A | 1 | a0012c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.359-5479C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432891 | ||||||
chr17:81432892
|
C | G | 9 | a0002c0001t0001g0136a0002c0001t0001g0169a0002c0001t0001g0174others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-5478C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432892 | ||||||
chr17:81432907
|
C | A | 42 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5463C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432907 | ||||||
chr17:81432909
|
C | T | 1 | a0002c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.359-5461C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432909 | ||||||
chr17:81432910
|
T | G | 101 | a0001c0003t0003g0048a0001c0003t0003g0068a0001c0003t0003g0083others(98): Show | 103 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.359-5460T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432910 | ||||||
chr17:81432910
|
T | TC | 40 | a0001c0003t0003g0286a0001c0007t0009g0260a0001c0007t0016g0234others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.359-5460_359-5459i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432910 | ||||||
chr17:81432911
|
T | C | 42 | a0001c0003t0003g0286a0001c0007t0009g0014a0001c0007t0009g0260others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5459T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432911 | ||||||
chr17:81432911
|
T | TCCCCCCA others(18): Show |
10 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(7): Show | 10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-5444_359-5443i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432911 | |||||
chr17:81432917
|
C | CATCCCCA others(18): Show |
1 | a0006c0020t0002g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359-5444_359-5443i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432917 | |||||
chr17:81433072
|
G | A | 1 | a0001c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.359-5298G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433072 | ||||||
chr17:81433133
|
G | C | 18 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(15): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.359-5237G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433133 | ||||||
chr17:81433216
|
G | C | 36 | a0001c0003t0003g0110a0001c0007t0015g0275a0001c0012t0002g0112others(33): Show | 36 | HG00544.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.359-5154G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433216 | ||||||
chr17:81433423
|
T | C | 21 | a0001c0003t0003g0208a0001c0003t0003g0293a0001c0010t0004g0296others(18): Show | 22 | HG00408.hp1 HG01069.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.359-4947T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433423 | ||||||
chr17:81433510
|
T | C | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4860T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433510 | ||||||
chr17:81433523
|
A | C | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4847A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433523 | ||||||
chr17:81433554
|
T | C | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-4816T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433554 | ||||||
chr17:81433562
|
T | C | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4808T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433562 | ||||||
chr17:81433563
|
T | C | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4807T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433563 | ||||||
chr17:81433564
|
A | C | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4806A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433564 | ||||||
chr17:81433576
|
A | G | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4794A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433576 | ||||||
chr17:81433595
|
C | T | 10 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(7): Show | 10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-4775C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433595 | ||||||
chr17:81433671
|
G | A | 2 | a0013c0027t0001g0025a0013c0027t0001g0026 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.359-4699G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433671 | ||||||
chr17:81433708
|
G | A | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4662G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433708 | ||||||
chr17:81433727
|
G | A | 6 | a0002c0001t0001g0169a0003c0002t0004g0170a0003c0002t0004g0171others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-4643G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433727 | ||||||
chr17:81433748
|
C | T | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-4622C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433748 | ||||||
chr17:81433757
|
C | T | 17 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.359-4613C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433757 | ||||||
chr17:81433869
|
A | G | 4 | a0001c0094t0009g0016a0015c0014t0001g0243a0016c0030t0007g0032others(1): Show | 4 | HG00639.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-4501A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433869 | ||||||
chr17:81433990
|
G | A | 8 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0012t0002g0133others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-4380G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433990 | ||||||
chr17:81434023
|
C | T | 3 | a0002c0001t0002g0132a0009c0013t0006g0029a0009c0013t0006g0140 | 3 | HG03017.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.359-4347C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434023 | ||||||
chr17:81434070
|
C | T | 2 | a0005c0005t0005g0202a0005c0096t0005g0199 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.359-4300C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434070 | ||||||
chr17:81434216
|
C | T | 11 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0012t0002g0133others(8): Show | 11 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-4154C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434216 | ||||||
chr17:81434248
|
C | T | 1 | a0006c0020t0002g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359-4122C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434248 | ||||||
chr17:81434291
|
A | T | 8 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0012t0002g0133others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-4079A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434291 | ||||||
chr17:81434313
|
C | T | 1 | a0013c0097t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359-4057C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434313 | ||||||
chr17:81434355
|
G | A | 3 | a0002c0001t0001g0320a0014c0022t0011g0322a0014c0022t0011g0323 | 3 | HG01884.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.359-4015G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434355 | ||||||
chr17:81434365
|
C | T | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-4005C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434365 | ||||||
chr17:81434396
|
A | G | 8 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0012t0002g0133others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-3974A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434396 | ||||||
chr17:81434413
|
G | A | 1 | a0003c0002t0004g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.359-3957G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434413 | ||||||
chr17:81434447
|
G | T | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-3923G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434447 | ||||||
chr17:81434463
|
C | T | 1 | a0007c0008t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.359-3907C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434463 | ||||||
chr17:81434487
|
G | A | 1 | a0009c0013t0006g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.359-3883G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434487 | ||||||
chr17:81434656
|
C | T | 3 | a0001c0069t0007g0253a0010c0031t0004g0015a0030c0090t0002g0265 | 3 | HG02451.hp1 HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.359-3714C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434656 | ||||||
chr17:81434739
|
C | A | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-3631C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434739 | ||||||
chr17:81434741
|
G | C | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-3629G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434741 | ||||||
chr17:81434744
|
T | G | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-3626T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434744 | ||||||
chr17:81434906
|
C | T | 1 | a0002c0001t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.359-3464C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434906 | ||||||
chr17:81434946
|
C | G | 1 | a0002c0001t0001g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.359-3424C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434946 | ||||||
chr17:81435036
|
C | G | 1 | a0057c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.359-3334C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435036 | ||||||
chr17:81435107
|
A | G | 1 | a0005c0005t0008g0298 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.359-3263A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435107 | ||||||
chr17:81435117
|
A | C | 1 | a0004c0004t0002g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359-3253A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435117 | ||||||
chr17:81435142
|
C | T | 1 | a0002c0016t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.359-3228C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435142 | ||||||
chr17:81435219
|
G | A | 2 | a0001c0007t0009g0014a0001c0007t0016g0161 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.359-3151G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435219 | ||||||
chr17:81435347
|
G | A | 16 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(13): Show | 17 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.359-3023G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435347 | ||||||
chr17:81435389
|
A | C | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-2981A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435389 | ||||||
chr17:81435399
|
G | A | 1 | a0025c0107t0002g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.359-2971G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435399 | ||||||
chr17:81435402
|
C | T | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.359-2968C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435402 | ||||||
chr17:81435458
|
G | C | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-2912G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435458 | ||||||
chr17:81435488
|
C | T | 32 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(29): Show | 32 | HG00673.hp1 HG01109.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.359-2882C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435488 | ||||||
chr17:81435577
|
C | T | 11 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-2793C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435577 | ||||||
chr17:81435672
|
G | A | 1 | a0015c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.359-2698G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435672 | ||||||
chr17:81435756
|
A | C | 1 | a0002c0001t0005g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.359-2614A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435756 | ||||||
chr17:81435923
|
C | A | 2 | a0001c0009t0024g0248a0001c0009t0025g0252 | 2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.359-2447C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435923 | ||||||
chr17:81435937
|
CTTTCTCA others(3): Show |
C | 1 | a0012c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.359-2430_359-2421d others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81435937 | |||||
chr17:81436058
|
G | C | 2 | a0001c0103t0026g0245a0007c0008t0004g0317 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.359-2312G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436058 | ||||||
chr17:81436135
|
T | C | 75 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0009g0260others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.359-2235T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436135 | ||||||
chr17:81436179
|
C | T | 6 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0021t0002g0077others(3): Show | 6 | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-2191C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436179 | ||||||
chr17:81436237
|
T | C | 40 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0015g0275others(37): Show | 41 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.359-2133T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436237 | ||||||
chr17:81436262
|
G | A | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.359-2108G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436262 | ||||||
chr17:81436332
|
C | T | 1 | a0024c0082t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.359-2038C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436332 | ||||||
chr17:81436345
|
C | T | 1 | a0001c0003t0003g0293 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.359-2025C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436345 | ||||||
chr17:81436378
|
G | C | 121 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(118): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.359-1992G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436378 | ||||||
chr17:81436379
|
C | A | 1 | a0008c0073t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.359-1991C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436379 | ||||||
chr17:81436410
|
C | G | 3 | a0007c0008t0001g0005a0007c0008t0001g0021a0015c0014t0001g0001 | 4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1960C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436410 | ||||||
chr17:81436416
|
G | A | 3 | a0007c0008t0001g0005a0007c0008t0001g0021a0015c0014t0001g0001 | 4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1954G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436416 | ||||||
chr17:81436437
|
T | C | 1 | a0001c0093t0001g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.359-1933T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436437 | ||||||
chr17:81436497
|
G | A | 2 | a0002c0001t0001g0321a0002c0076t0001g0303 | 2 | NA18962.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.359-1873G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436497 | ||||||
chr17:81436596
|
G | A | 1 | a0001c0094t0009g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.359-1774G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436596 | ||||||
chr17:81436617
|
G | A | 2 | a0009c0013t0006g0029a0009c0013t0006g0140 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.359-1753G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436617 | ||||||
chr17:81436638
|
A | C | 35 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(32): Show | 35 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.359-1732A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436638 | ||||||
chr17:81436707
|
G | A | 1 | a0003c0002t0004g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.359-1663G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436707 | ||||||
chr17:81436733
|
G | A | 17 | a0001c0007t0033g0135a0001c0010t0001g0034a0001c0026t0003g0246others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.359-1637G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436733 | ||||||
chr17:81436896
|
A | T | 1 | a0033c0067t0001g0305 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.359-1474A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436896 | ||||||
chr17:81436906
|
C | T | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.359-1464C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436906 | ||||||
chr17:81436920
|
A | G | 35 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(32): Show | 35 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.359-1450A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436920 | ||||||
chr17:81436958
|
G | A | 1 | a0004c0004t0002g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.359-1412G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436958 | ||||||
chr17:81437074
|
G | A | 1 | a0004c0004t0002g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.359-1296G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437074 | ||||||
chr17:81437156
|
C | T | 1 | a0001c0003t0003g0050 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.359-1214C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437156 | ||||||
chr17:81437433
|
G | C | 1 | a0010c0031t0004g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.359-937G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437433 | ||||||
chr17:81437436
|
T | C | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-934T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437436 | ||||||
chr17:81437513
|
C | T | 1 | a0003c0002t0013g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.359-857C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437513 | ||||||
chr17:81437660
|
C | T | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.359-710C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437660 | ||||||
chr17:81437731
|
G | A | 1 | a0049c0098t0002g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-639G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437731 | ||||||
chr17:81437819
|
C | T | 1 | a0001c0003t0003g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.359-551C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437819 | ||||||
chr17:81437960
|
G | C | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-410G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437960 | ||||||
chr17:81438085
|
G | A | 1 | a0049c0098t0002g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-285G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81438085 | ||||||
chr17:81438192
|
T | G | 1 | a0004c0011t0002g0162 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.359-178T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81438192 | ||||||
chr17:81438328
|
G | A | 1 | a0001c0021t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.359-42G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81438328 | ||||||
chr17:81438511
|
C | T | 8 | a0004c0004t0002g0003a0004c0004t0002g0266a0004c0004t0002g0269others(5): Show | 9 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+19C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438511 | ||||||
chr17:81438658
|
G | T | 10 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(7): Show | 10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+166G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438658 | ||||||
chr17:81438683
|
A | G | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.481+191A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438683 | ||||||
chr17:81438692
|
C | T | 21 | a0001c0009t0037g0319a0003c0018t0002g0143a0004c0004t0002g0003others(18): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+200C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438692 | ||||||
chr17:81438730
|
CTCACTGC others(39): Show |
C | 1 | a0002c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.481+239_481+284del others(46): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438730 | ||||||
chr17:81438793
|
G | A | 2 | a0001c0009t0024g0248a0001c0009t0025g0252 | 2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.481+301G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438793 | ||||||
chr17:81438905
|
A | G | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.481+413A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438905 | ||||||
chr17:81439016
|
C | T | 11 | a0001c0009t0004g0117a0001c0012t0002g0137a0002c0001t0002g0012others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.481+524C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439016 | ||||||
chr17:81439122
|
C | A | 31 | a0001c0007t0009g0260a0001c0007t0016g0234a0001c0009t0037g0319others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.481+630C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439122 | ||||||
chr17:81439205
|
A | T | 1 | a0001c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.481+713A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439205 | ||||||
chr17:81439411
|
G | A | 10 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0021t0002g0077others(7): Show | 10 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+919G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439411 | ||||||
chr17:81439431
|
G | C | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.481+939G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439431 | ||||||
chr17:81439507
|
G | A | 9 | a0001c0003t0003g0231a0001c0003t0003g0233a0001c0032t0003g0232others(6): Show | 9 | HG00639.hp2 HG01175.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+1015G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439507 | ||||||
chr17:81439530
|
G | A | 49 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(46): Show | 49 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.481+1038G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439530 | ||||||
chr17:81439586
|
G | A | 3 | a0002c0001t0001g0035a0002c0001t0001g0036a0036c0061t0003g0189 | 3 | NA18747.hp1 NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.481+1094G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439586 | ||||||
chr17:81439665
|
C | G | 2 | a0001c0025t0003g0065a0001c0025t0003g0212 | 2 | HG02015.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.481+1173C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439665 | ||||||
chr17:81439674
|
C | T | 1 | a0003c0018t0001g0307 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.481+1182C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439674 | ||||||
chr17:81439757
|
G | A | 107 | a0001c0003t0003g0048a0001c0003t0003g0068a0001c0003t0003g0083others(104): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.481+1265G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439757 | ||||||
chr17:81439812
|
T | C | 16 | a0001c0007t0015g0275a0001c0069t0007g0253a0001c0101t0010g0020others(13): Show | 16 | HG01074.hp2 HG02451.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.481+1320T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439812 | ||||||
chr17:81439831
|
C | A | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.481+1339C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439831 | ||||||
chr17:81439943
|
G | GGCCTGCA others(7): Show |
2 | a0001c0007t0009g0014a0001c0007t0016g0161 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.481+1459_481+1472d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81439943 | |||||
chr17:81439956
|
T | A | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.481+1464T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439956 | ||||||
chr17:81439956
|
T | G | 111 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.481+1464T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439956 | ||||||
chr17:81439971
|
C | T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.481+1479C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439971 | ||||||
chr17:81440010
|
T | A | 132 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.481+1518T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440010 | ||||||
chr17:81440136
|
G | A | 1 | a0021c0079t0003g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.481+1644G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440136 | ||||||
chr17:81440713
|
C | T | 8 | a0001c0012t0002g0112a0005c0005t0005g0202a0005c0005t0012g0204others(5): Show | 8 | HG02083.hp2 HG03239.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-1118C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440713 | ||||||
chr17:81440726
|
T | C | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.482-1105T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440726 | ||||||
chr17:81440751
|
A | G | 2 | a0002c0001t0001g0091a0002c0001t0001g0187 | 2 | NA18947.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.482-1080A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440751 | ||||||
chr17:81440948
|
C | A | 1 | a0001c0009t0030g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.482-883C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440948 | ||||||
chr17:81441066
|
G | A | 304 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(301): Show | 308 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.482-765G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441066 | ||||||
chr17:81441199
|
G | A | 17 | a0001c0007t0016g0234a0001c0010t0009g0185a0001c0069t0007g0253others(14): Show | 17 | HG00140.hp2 HG01928.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-632G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441199 | ||||||
chr17:81441227
|
C | T | 24 | a0001c0007t0016g0234a0003c0002t0004g0295a0004c0004t0002g0003others(21): Show | 25 | HG00140.hp2 HG01243.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.482-604C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441227 | ||||||
chr17:81441233
|
G | A | 1 | a0011c0015t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.482-598G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441233 | ||||||
chr17:81441269
|
C | T | 1 | a0008c0029t0021g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-562C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441269 | ||||||
chr17:81441434
|
G | A | 3 | a0005c0005t0012g0204a0005c0005t0012g0206a0005c0005t0012g0207 | 3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.482-397G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441434 | ||||||
chr17:81441438
|
G | A | 1 | a0002c0001t0002g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.482-393G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441438 | ||||||
chr17:81441445
|
G | A | 1 | a0001c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.482-386G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441445 | ||||||
chr17:81441458
|
C | T | 12 | a0001c0003t0010g0211a0001c0007t0002g0007a0001c0007t0009g0014others(9): Show | 12 | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.482-373C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441458 | ||||||
chr17:81441487
|
C | T | 4 | a0001c0003t0003g0110a0001c0003t0003g0259a0001c0051t0001g0288others(1): Show | 4 | HG02074.hp2 HG02083.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-344C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441487 | ||||||
chr17:81441536
|
C | T | 2 | a0005c0005t0008g0297a0005c0005t0008g0298 | 2 | HG01069.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.482-295C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441536 | ||||||
chr17:81441655
|
C | T | 14 | a0001c0092t0004g0227a0005c0005t0005g0202a0005c0005t0008g0078others(11): Show | 14 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.482-176C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441655 | ||||||
chr17:81441668
|
C | CA | 76 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.482-141dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | |||||
chr17:81441668
|
C | CAA | 6 | a0001c0009t0006g0134a0001c0010t0001g0255a0001c0010t0004g0121others(3): Show | 6 | HG01261.hp1 HG01978.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-142_482-141dup others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | |||||
chr17:81441668
|
CA | C | 123 | a0001c0007t0009g0260a0001c0007t0016g0234a0001c0025t0003g0065others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.482-141delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | |||||
chr17:81441668
|
CAA | C | 6 | a0003c0002t0001g0213a0004c0004t0002g0003a0004c0004t0002g0269others(3): Show | 7 | HG01243.hp1 HG01891.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-142_482-141del others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | |||||
chr17:81441681
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.482-148_482-139del others(10): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441681 | |||||
chr17:81441753
|
T | A | 1 | a0012c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.482-78T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441753 | ||||||
chr17:81443602
|
A | T | 2 | a0016c0030t0007g0032a0016c0030t0007g0239 | 2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2215+38A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/27 | chr17 | 81443602 | ||||||
chr17:81443785
|
G | A | 11 | a0001c0093t0001g0145a0006c0006t0001g0009a0006c0006t0001g0150others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2216-24G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/27 | chr17 | 81443785 | ||||||
chr17:81444019
|
A | G | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2324+102A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444019 | ||||||
chr17:81444034
|
C | G | 1 | a0056c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2324+117C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444034 | ||||||
chr17:81444086
|
G | A | 11 | a0001c0092t0004g0227a0005c0005t0005g0202a0005c0005t0008g0078others(8): Show | 11 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.2324+169G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444086 | ||||||
chr17:81444217
|
C | T | 78 | a0001c0007t0002g0007a0001c0007t0009g0014a0001c0007t0033g0135others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.2325-164C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444217 | ||||||
chr17:81444324
|
T | G | 1 | a0002c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2325-57T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444324 | ||||||
chr17:81444636
|
G | A | 42 | a0003c0018t0002g0143a0004c0004t0002g0003a0004c0004t0002g0010others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.2513-32G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 7/27 | chr17 | 81444636 | ||||||
chr17:81444907
|
T | G | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2671+81T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/27 | chr17 | 81444907 | ||||||
chr17:81444942
|
A | G | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2672-73A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/27 | chr17 | 81444942 | ||||||
chr17:81445184
|
G | A | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.2835+6G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 9/27 | chr17 | 81445184 | ||||||
chr17:81445721
|
C | G | 1 | a0001c0003t0003g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3163+40C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445721 | ||||||
chr17:81445767
|
T | A | 1 | a0002c0057t0003g0284 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3163+86T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445767 | ||||||
chr17:81445859
|
T | A | 87 | a0001c0007t0015g0275a0001c0085t0001g0073a0003c0002t0001g0002others(84): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3163+178T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445859 | ||||||
chr17:81445917
|
G | A | 1 | a0002c0001t0001g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3163+236G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445917 | ||||||
chr17:81445935
|
C | T | 2 | a0001c0007t0016g0161a0001c0103t0026g0245 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3163+254C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445935 | ||||||
chr17:81445946
|
G | A | 1 | a0008c0029t0021g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3163+265G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445946 | ||||||
chr17:81445968
|
G | A | 1 | a0004c0004t0002g0010 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3163+287G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445968 | ||||||
chr17:81446031
|
T | A | 9 | a0001c0007t0009g0014a0001c0009t0006g0134a0001c0009t0030g0263others(6): Show | 9 | HG01261.hp1 HG01515.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3163+350T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446031 | ||||||
chr17:81446039
|
A | G | 5 | a0001c0009t0006g0134a0009c0013t0006g0029a0009c0013t0006g0140others(2): Show | 5 | HG01261.hp1 HG01515.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.3163+358A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446039 | ||||||
chr17:81446086
|
C | A | 86 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.3163+405C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446086 | ||||||
chr17:81446096
|
G | C | 5 | a0001c0007t0002g0007a0001c0021t0002g0077a0001c0021t0002g0114others(2): Show | 5 | HG00099.hp2 HG00733.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163+415G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446096 | ||||||
chr17:81446128
|
C | T | 1 | a0001c0019t0003g0294 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3163+447C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446128 | ||||||
chr17:81446144
|
A | G | 67 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(64): Show | 67 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3163+463A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446144 | ||||||
chr17:81446253
|
G | A | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3163+572G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446253 | ||||||
chr17:81446283
|
T | A | 1 | a0008c0073t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3163+602T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446283 | ||||||
chr17:81446410
|
T | C | 221 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.3164-626T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446410 | ||||||
chr17:81446449
|
C | A | 219 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(216): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.3164-587C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446449 | ||||||
chr17:81446464
|
T | C | 1 | a0001c0094t0009g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3164-572T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446464 | ||||||
chr17:81446467
|
G | A | 2 | a0001c0007t0016g0161a0001c0103t0026g0245 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3164-569G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446467 | ||||||
chr17:81446526
|
C | CT | 75 | a0001c0012t0002g0159a0002c0001t0001g0004a0002c0001t0001g0037others(72): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.3164-472dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
C | CTT | 48 | a0002c0001t0001g0028a0002c0001t0001g0033a0002c0001t0001g0136others(45): Show | 49 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.3164-473_3164-472d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
C | CTTT | 15 | a0001c0085t0001g0073a0002c0001t0001g0030a0002c0001t0005g0064others(12): Show | 15 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3164-474_3164-472d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
C | CTTTTTTT others(9): Show |
1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3164-487_3164-472d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CT | C | 14 | a0001c0012t0002g0058a0001c0012t0002g0112a0001c0012t0002g0137others(11): Show | 14 | HG01069.hp1 HG01123.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.3164-472delT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3164-482_3164-472d others(13): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(6): Show |
C | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3164-484_3164-472d others(15): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0003t0003g0184a0001c0003t0003g0230a0001c0003t0003g0259others(2): Show | 5 | HG01516.hp2 NA18950.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.3164-485_3164-472d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(8): Show |
C | 57 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(54): Show | 57 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.3164-486_3164-472d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(9): Show |
C | 5 | a0001c0003t0003g0068a0001c0003t0003g0290a0001c0003t0010g0211others(2): Show | 5 | HG00323.hp1 HG01070.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.3164-487_3164-472d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0009t0030g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3164-488_3164-472d others(19): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(11): Show |
C | 32 | a0001c0007t0002g0007a0001c0007t0009g0014a0001c0007t0009g0260others(29): Show | 32 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.3164-489_3164-472d others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446526
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0009t0004g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3164-494_3164-472d others(25): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | |||||
chr17:81446655
|
C | T | 2 | a0047c0046t0004g0273a0048c0045t0001g0254 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3164-381C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446655 | ||||||
chr17:81446699
|
C | T | 2 | a0001c0007t0016g0161a0001c0103t0026g0245 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3164-337C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446699 | ||||||
chr17:81446898
|
T | C | 43 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(40): Show | 44 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.3164-138T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446898 | ||||||
chr17:81446928
|
C | T | 25 | a0001c0007t0002g0007a0001c0009t0006g0134a0001c0021t0002g0077others(22): Show | 26 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3164-108C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446928 | ||||||
chr17:81446933
|
G | A | 1 | a0008c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3164-103G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446933 | ||||||
chr17:81446995
|
A | G | 2 | a0001c0007t0016g0161a0001c0103t0026g0245 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3164-41A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446995 | ||||||
chr17:81447870
|
A | AC | 7 | a0001c0003t0003g0208a0001c0003t0003g0286a0001c0021t0002g0262others(4): Show | 7 | HG01496.hp2 HG02300.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3976+28dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr17 | 81447870 | |||||
chr17:81447871
|
C | A | 90 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.3976+23C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447871 | ||||||
chr17:81447888
|
A | G | 219 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(216): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.3976+40A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447888 | ||||||
chr17:81447902
|
G | A | 1 | a0014c0022t0011g0322 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3976+54G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447902 | ||||||
chr17:81447928
|
C | T | 6 | a0007c0008t0001g0005a0007c0008t0001g0021a0007c0008t0001g0257others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3976+80C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447928 | ||||||
chr17:81448119
|
C | T | 1 | a0003c0002t0001g0111 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3976+271C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448119 | ||||||
chr17:81448157
|
G | A | 1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3976+309G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448157 | ||||||
chr17:81448201
|
T | A | 2 | a0001c0007t0009g0014a0001c0094t0009g0016 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3976+353T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448201 | ||||||
chr17:81448229
|
C | T | 1 | a0001c0007t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3976+381C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448229 | ||||||
chr17:81448296
|
G | A | 2 | a0014c0022t0011g0322a0014c0022t0011g0323 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3976+448G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448296 | ||||||
chr17:81448324
|
A | G | 1 | a0001c0025t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3976+476A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448324 | ||||||
chr17:81448360
|
C | T | 173 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(170): Show | 175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.3976+512C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448360 | ||||||
chr17:81448369
|
C | T | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3976+521C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448369 | ||||||
chr17:81448388
|
C | T | 5 | a0010c0031t0004g0015a0010c0031t0004g0018a0010c0102t0004g0017others(2): Show | 5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3976+540C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448388 | ||||||
chr17:81448431
|
G | A | 1 | a0003c0002t0001g0107 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3976+583G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448431 | ||||||
chr17:81448557
|
G | T | 1 | a0002c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3976+709G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448557 | ||||||
chr17:81448569
|
C | T | 1 | a0003c0002t0004g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3976+721C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448569 | ||||||
chr17:81448582
|
G | A | 3 | a0002c0063t0020g0251a0019c0105t0001g0249a0057c0104t0010g0160 | 3 | HG02809.hp1 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3976+734G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448582 | ||||||
chr17:81448599
|
G | A | 1 | a0002c0057t0003g0284 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3976+751G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448599 | ||||||
chr17:81448599
|
G | T | 1 | a0004c0004t0029g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3976+751G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448599 | ||||||
chr17:81448626
|
G | A | 28 | a0001c0007t0002g0007a0001c0007t0009g0014a0001c0009t0006g0134others(25): Show | 28 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.3976+778G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448626 | ||||||
chr17:81448740
|
G | A | 89 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(86): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.3976+892G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448740 | ||||||
chr17:81448838
|
G | A | 1 | a0001c0007t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3976+990G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448838 | ||||||
chr17:81448874
|
A | AC | 28 | a0001c0007t0002g0007a0001c0007t0009g0014a0001c0009t0006g0134others(25): Show | 28 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.3976+1032dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr17 | 81448874 | |||||
chr17:81448947
|
C | G | 91 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3976+1099C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448947 | ||||||
chr17:81448978
|
G | A | 1 | a0001c0003t0003g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3976+1130G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448978 | ||||||
chr17:81449055
|
C | T | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3976+1207C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449055 | ||||||
chr17:81449089
|
G | C | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3976+1241G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449089 | ||||||
chr17:81449101
|
G | A | 1 | a0001c0010t0004g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3976+1253G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449101 | ||||||
chr17:81449177
|
C | T | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3976+1329C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449177 | ||||||
chr17:81449187
|
C | T | 11 | a0006c0006t0001g0009a0006c0006t0001g0150a0006c0006t0001g0151others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3976+1339C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449187 | ||||||
chr17:81449207
|
A | G | 57 | a0001c0007t0002g0007a0001c0007t0009g0014a0001c0007t0009g0260others(54): Show | 57 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3976+1359A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449207 | ||||||
chr17:81449263
|
C | T | 9 | a0004c0004t0002g0003a0004c0004t0002g0266a0004c0004t0002g0269others(6): Show | 10 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.3976+1415C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449263 | ||||||
chr17:81449316
|
G | A | 1 | a0002c0074t0001g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3976+1468G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449316 | ||||||
chr17:81449428
|
A | G | 221 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.3976+1580A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449428 | ||||||
chr17:81449630
|
T | C | 91 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3976+1782T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449630 | ||||||
chr17:81449646
|
C | T | 2 | a0047c0046t0004g0273a0048c0045t0001g0254 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3976+1798C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449646 | ||||||
chr17:81449681
|
C | G | 1 | a0003c0018t0002g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3976+1833C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449681 | ||||||
chr17:81449686
|
G | A | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3976+1838G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449686 | ||||||
chr17:81449805
|
C | T | 1 | a0039c0058t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3977-1863C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449805 | ||||||
chr17:81449817
|
G | A | 1 | a0003c0064t0005g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3977-1851G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449817 | ||||||
chr17:81449990
|
G | A | 1 | a0001c0009t0030g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3977-1678G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449990 | ||||||
chr17:81450069
|
G | A | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3977-1599G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450069 | ||||||
chr17:81450282
|
G | A | 10 | a0001c0009t0004g0117a0001c0012t0002g0058a0001c0012t0002g0112others(7): Show | 10 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.3977-1386G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450282 | ||||||
chr17:81450374
|
G | A | 61 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(58): Show | 61 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.3977-1294G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450374 | ||||||
chr17:81450378
|
C | A | 11 | a0006c0006t0001g0009a0006c0006t0001g0150a0006c0006t0001g0151others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3977-1290C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450378 | ||||||
chr17:81450387
|
C | T | 5 | a0009c0013t0006g0029a0009c0013t0006g0140a0013c0027t0001g0025others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3977-1281C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450387 | ||||||
chr17:81450406
|
A | C | 1 | a0001c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1262A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450406 | ||||||
chr17:81450457
|
G | A | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3977-1211G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450457 | ||||||
chr17:81450502
|
T | C | 220 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(217): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.3977-1166T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450502 | ||||||
chr17:81450502
|
T | G | 1 | a0001c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1166T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450502 | ||||||
chr17:81450503
|
G | T | 1 | a0001c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1165G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450503 | ||||||
chr17:81450504
|
T | C | 1 | a0001c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1164T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450504 | ||||||
chr17:81450607
|
G | A | 1 | a0004c0011t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3977-1061G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450607 | ||||||
chr17:81450755
|
C | T | 3 | a0010c0031t0004g0015a0010c0031t0004g0018a0010c0102t0004g0017 | 3 | HG02258.hp2 HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3977-913C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450755 | ||||||
chr17:81450923
|
G | A | 17 | a0001c0003t0003g0050a0001c0003t0003g0110a0001c0003t0003g0258others(14): Show | 17 | HG01433.hp2 HG01943.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3977-745G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450923 | ||||||
chr17:81450960
|
C | A | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3977-708C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450960 | ||||||
chr17:81451158
|
C | T | 1 | a0016c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3977-510C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451158 | ||||||
chr17:81451230
|
G | A | 3 | a0002c0001t0001g0281a0002c0001t0001g0282a0002c0055t0005g0283 | 3 | HG02027.hp1 HG02071.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3977-438G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451230 | ||||||
chr17:81451234
|
A | G | 221 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.3977-434A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451234 | ||||||
chr17:81451311
|
C | T | 7 | a0003c0002t0004g0170a0003c0002t0004g0171a0003c0002t0004g0172others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3977-357C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451311 | ||||||
chr17:81451400
|
C | T | 2 | a0008c0024t0001g0175a0008c0024t0001g0306 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3977-268C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451400 | ||||||
chr17:81451573
|
C | T | 91 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3977-95C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451573 | ||||||
chr17:81451899
|
C | T | 4 | a0001c0007t0016g0234a0001c0007t0033g0135a0047c0046t0004g0273others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4179+29C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/27 | chr17 | 81451899 | ||||||
chr17:81451957
|
G | GC | 81 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(78): Show |
splice_region_variant&intron_variant | LOW | c.4180-6dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr17 | 81451957 | |||||
chr17:81452132
|
C | G | 43 | a0001c0007t0002g0007a0001c0007t0009g0014a0001c0007t0009g0260others(40): Show | 43 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.4316+25C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452132 | ||||||
chr17:81452133
|
TGGGAGGG others(19): Show |
T | 97 | a0001c0007t0015g0275a0001c0007t0016g0234a0001c0007t0033g0135others(94): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.4316+33_4316+58del others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr17 | 81452133 | |||||
chr17:81452292
|
C | A | 6 | a0001c0007t0009g0260a0001c0009t0024g0248a0001c0009t0025g0252others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4316+185C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452292 | ||||||
chr17:81452292
|
C | T | 1 | a0003c0064t0005g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4316+185C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452292 | ||||||
chr17:81452392
|
G | A | 62 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(59): Show | 62 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.4316+285G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452392 | ||||||
chr17:81452668
|
T | G | 1 | a0004c0004t0002g0010 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4317-55T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452668 | ||||||
chr17:81452711
|
T | C | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4317-12T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452711 | ||||||
chr17:81452929
|
T | C | 1 | a0041c0053t0001g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4445+78T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81452929 | ||||||
chr17:81452969
|
A | C | 11 | a0006c0006t0001g0009a0006c0006t0001g0150a0006c0006t0001g0151others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4445+118A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81452969 | ||||||
chr17:81453158
|
C | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4445+307C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453158 | ||||||
chr17:81453198
|
C | G | 91 | a0001c0009t0004g0117a0001c0085t0001g0073a0003c0002t0001g0002others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.4445+347C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453198 | ||||||
chr17:81453253
|
C | T | 5 | a0001c0007t0009g0260a0001c0009t0024g0248a0001c0009t0025g0252others(2): Show | 5 | HG01261.hp2 HG02056.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4445+402C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453253 | ||||||
chr17:81453411
|
G | T | 5 | a0010c0031t0004g0015a0010c0031t0004g0018a0010c0102t0004g0017others(2): Show | 5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4445+560G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453411 | ||||||
chr17:81453591
|
G | GC | 92 | a0001c0009t0025g0252a0001c0009t0030g0263a0001c0009t0037g0319others(89): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4445+749dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr17 | 81453591 | |||||
chr17:81453635
|
G | T | 1 | a0046c0047t0027g0264 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4445+784G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453635 | ||||||
chr17:81453676
|
C | T | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4445+825C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453676 | ||||||
chr17:81453730
|
GGCA | G | 11 | a0006c0006t0001g0009a0006c0006t0001g0150a0006c0006t0001g0151others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4445+885_4445+887d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr17 | 81453730 | |||||
chr17:81453829
|
C | T | 1 | a0004c0037t0014g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4445+978C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453829 | ||||||
chr17:81453894
|
C | T | 1 | a0006c0006t0002g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4445+1043C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453894 | ||||||
chr17:81453912
|
T | C | 1 | a0048c0045t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4445+1061T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453912 | ||||||
chr17:81453976
|
G | A | 19 | a0001c0007t0002g0007a0001c0021t0002g0077a0001c0021t0002g0114others(16): Show | 19 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.4445+1125G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453976 | ||||||
chr17:81454091
|
G | A | 2 | a0006c0020t0002g0238a0006c0020t0002g0325 | 2 | HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.4446-1176G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454091 | ||||||
chr17:81454116
|
C | T | 1 | a0008c0029t0021g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4446-1151C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454116 | ||||||
chr17:81454228
|
G | T | 128 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(125): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.4446-1039G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454228 | ||||||
chr17:81454240
|
G | A | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4446-1027G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454240 | ||||||
chr17:81454446
|
G | A | 1 | a0001c0025t0003g0065 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4446-821G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454446 | ||||||
chr17:81454448
|
G | A | 4 | a0001c0007t0016g0234a0001c0007t0033g0135a0047c0046t0004g0273others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-819G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454448 | ||||||
chr17:81454508
|
CAG | C | 4 | a0001c0007t0009g0260a0001c0009t0024g0248a0001c0009t0025g0252others(1): Show | 4 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-758_4446-757d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454508 | ||||||
chr17:81454539
|
C | CCCCCA | 11 | a0006c0006t0001g0009a0006c0006t0001g0150a0006c0006t0001g0151others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4446-714_4446-710d others(7): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr17 | 81454539 | |||||
chr17:81454558
|
A | G | 217 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.4446-709A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454558 | ||||||
chr17:81454573
|
C | T | 1 | a0002c0001t0001g0320 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4446-694C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454573 | ||||||
chr17:81454600
|
G | A | 2 | a0002c0001t0001g0004a0019c0036t0001g0019 | 3 | HG02622.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4446-667G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454600 | ||||||
chr17:81454652
|
G | A | 1 | a0001c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4446-615G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454652 | ||||||
chr17:81454779
|
G | A | 1 | a0019c0105t0001g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4446-488G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454779 | ||||||
chr17:81454867
|
C | T | 1 | a0001c0007t0002g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4446-400C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454867 | ||||||
chr17:81454868
|
G | A | 1 | a0008c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4446-399G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454868 | ||||||
chr17:81454983
|
C | T | 3 | a0014c0022t0011g0322a0014c0022t0011g0323a0014c0022t0036g0318 | 3 | HG02647.hp2 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4446-284C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454983 | ||||||
chr17:81455016
|
G | A | 4 | a0001c0007t0009g0260a0001c0009t0024g0248a0001c0009t0025g0252others(1): Show | 4 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-251G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455016 | ||||||
chr17:81455087
|
CAGA | C | 4 | a0001c0007t0009g0260a0001c0009t0024g0248a0001c0009t0025g0252others(1): Show | 4 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-179_4446-177d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455087 | ||||||
chr17:81455154
|
G | C | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4446-113G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455154 | ||||||
chr17:81455226
|
G | A | 90 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.4446-41G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455226 | ||||||
chr17:81455263
|
C | T | 90 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
splice_region_variant&intron_variant | LOW | c.4446-4C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455263 | ||||||
chr17:81455400
|
G | A | 1 | a0001c0007t0009g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4569+10G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455400 | ||||||
chr17:81455457
|
T | G | 2 | a0002c0001t0001g0004a0019c0036t0001g0019 | 3 | HG02622.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4569+67T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455457 | ||||||
chr17:81455529
|
C | T | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4569+139C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455529 | ||||||
chr17:81455530
|
G | A | 1 | a0014c0022t0011g0322 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4569+140G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455530 | ||||||
chr17:81455628
|
G | A | 3 | a0005c0005t0008g0297a0005c0005t0008g0298a0028c0089t0001g0261 | 3 | HG01069.hp2 HG01934.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4569+238G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455628 | ||||||
chr17:81455675
|
A | G | 2 | a0047c0046t0004g0273a0048c0045t0001g0254 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.4569+285A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455675 | ||||||
chr17:81455779
|
G | C | 1 | a0005c0005t0008g0298 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4569+389G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455779 | ||||||
chr17:81455895
|
C | T | 1 | a0017c0023t0015g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4570-402C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455895 | ||||||
chr17:81455986
|
T | C | 1 | a0008c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4570-311T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455986 | ||||||
chr17:81456033
|
A | C | 3 | a0003c0002t0004g0280a0003c0002t0004g0295a0003c0064t0005g0198 | 3 | NA18612.hp1 NA18942.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.4570-264A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81456033 | ||||||
chr17:81456202
|
C | T | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4570-95C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81456202 | ||||||
chr17:81456623
|
C | T | 1 | a0001c0007t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4858+38C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81456623 | ||||||
chr17:81456716
|
G | A | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4858+131G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81456716 | ||||||
chr17:81456799
|
C | T | 5 | a0010c0031t0004g0015a0010c0031t0004g0018a0010c0102t0004g0017others(2): Show | 5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4858+214C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81456799 | ||||||
chr17:81456945
|
AC | A | 203 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.4858+368delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr17 | 81456945 | |||||
chr17:81457102
|
G | A | 90 | a0001c0085t0001g0073a0003c0002t0001g0002a0003c0002t0001g0039others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.4859-308G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457102 | ||||||
chr17:81457221
|
C | G | 1 | a0002c0001t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4859-189C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457221 | ||||||
chr17:81457258
|
C | T | 2 | a0015c0014t0001g0001a0015c0014t0001g0243 | 3 | HG00639.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4859-152C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457258 | ||||||
chr17:81457369
|
C | G | 1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4859-41C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457369 | ||||||
chr17:81457577
|
A | AGGCAGGG others(23): Show |
1 | a0027c0088t0004g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5028_5041+16dupGCA others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr17 | 81457577 | |||||
chr17:81457605
|
G | A | 7 | a0006c0006t0001g0009a0006c0006t0001g0150a0006c0006t0001g0151others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.5041+13G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457605 | ||||||
chr17:81457862
|
T | C | 327 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.5041+270T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457862 | ||||||
chr17:81457904
|
AGGGAGGG others(52): Show |
A | 4 | a0003c0002t0001g0049a0003c0002t0004g0280a0003c0002t0004g0295others(1): Show | 4 | NA18612.hp1 NA18942.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.5042-204_5042-146d others(61): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr17 | 81457904 | |||||
chr17:81457939
|
G | C | 1 | a0006c0020t0002g0325 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5042-226G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457939 | ||||||
chr17:81457960
|
C | T | 1 | a0018c0106t0010g0328 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5042-205C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457960 | ||||||
chr17:81457994
|
G | C | 3 | a0012c0017t0001g0228a0012c0017t0001g0301a0043c0077t0001g0094 | 3 | HG01106.hp2 HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.5042-171G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457994 | ||||||
chr17:81458066
|
G | T | 1 | a0031c0091t0001g0042 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5042-99G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81458066 | ||||||
chr17:81458115
|
C | T | 56 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(53): Show | 56 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.5042-50C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81458115 | ||||||
chr17:81458482
|
G | A | 1 | a0007c0008t0001g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5343+16G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458482 | ||||||
chr17:81458507
|
G | A | 2 | a0001c0007t0016g0161a0001c0103t0026g0245 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.5343+41G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458507 | ||||||
chr17:81458529
|
C | T | 3 | a0005c0005t0012g0204a0005c0005t0012g0206a0005c0005t0012g0207 | 3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5343+63C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458529 | ||||||
chr17:81458532
|
C | CCTCCCCC others(3): Show |
93 | a0001c0007t0016g0161a0001c0007t0016g0234a0001c0007t0033g0135others(90): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.5343+68_5343+77dup others(10): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr17 | 81458532 | |||||
chr17:81458532
|
C | CCTCCCCC others(13): Show |
1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5343+77_5344-77ins others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr17 | 81458532 | |||||
chr17:81458583
|
C | T | 10 | a0001c0009t0004g0117a0001c0012t0002g0058a0001c0012t0002g0112others(7): Show | 10 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.5344-38C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458583 | ||||||
chr17:81458614
|
C | T | 10 | a0001c0009t0004g0117a0001c0012t0002g0058a0001c0012t0002g0112others(7): Show | 10 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.5344-7C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458614 | ||||||
chr17:81458995
|
GC | G | 40 | a0003c0018t0002g0143a0003c0018t0002g0210a0004c0004t0002g0003others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.5605+28delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr17 | 81458995 | |||||
chr17:81458997
|
C | T | 4 | a0001c0010t0009g0185a0001c0069t0007g0253a0001c0101t0010g0020others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5605+28C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/27 | chr17 | 81458997 | ||||||
chr17:81459029
|
G | A | 1 | a0047c0046t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5606-25G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/27 | chr17 | 81459029 | ||||||
chr17:81459235
|
A | G | 1 | a0004c0004t0029g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5721-18A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 21/27 | chr17 | 81459235 | ||||||
chr17:81459340
|
G | T | 2 | a0015c0014t0001g0001a0015c0014t0001g0243 | 3 | HG00639.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5796+12G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459340 | ||||||
chr17:81459342
|
C | T | 1 | a0025c0107t0002g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5796+14C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459342 | ||||||
chr17:81459356
|
G | A | 1 | a0002c0001t0002g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5796+28G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459356 | ||||||
chr17:81459390
|
A | G | 92 | a0001c0012t0002g0058a0001c0012t0002g0159a0003c0002t0001g0002others(89): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.5796+62A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459390 | ||||||
chr17:81459455
|
A | G | 206 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.5797-41A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459455 | ||||||
chr17:81459682
|
C | G | 118 | a0001c0068t0008g0070a0001c0085t0001g0073a0002c0001t0001g0004others(115): Show | 120 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.5905+78C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459682 | ||||||
chr17:81459730
|
C | T | 82 | a0003c0002t0001g0002a0003c0002t0001g0039a0003c0002t0001g0049others(79): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.5905+126C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459730 | ||||||
chr17:81459785
|
G | C | 1 | a0001c0007t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5905+181G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459785 | ||||||
chr17:81459800
|
C | T | 1 | a0039c0058t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5905+196C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459800 | ||||||
chr17:81459913
|
C | T | 2 | a0001c0007t0016g0234a0001c0007t0033g0135 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5905+309C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459913 | ||||||
chr17:81459980
|
C | T | 2 | a0003c0002t0004g0170a0003c0002t0004g0171 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.5906-297C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459980 | ||||||
chr17:81459988
|
G | T | 1 | a0015c0014t0001g0001 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5906-289G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459988 | ||||||
chr17:81460028
|
G | C | 34 | a0001c0003t0003g0184a0001c0003t0003g0186a0002c0001t0001g0028others(31): Show | 34 | HG00423.hp1 HG00673.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.5906-249G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81460028 | ||||||
chr17:81460041
|
G | A | 1 | a0008c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5906-236G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81460041 | ||||||
chr17:81460232
|
G | A | 68 | a0001c0010t0001g0082a0002c0001t0001g0028a0002c0001t0001g0030others(65): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.5906-45G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81460232 | ||||||
chr17:81460481
|
G | C | 1 | a0005c0005t0008g0087 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6026-49G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/27 | chr17 | 81460481 | ||||||
chr17:81460501
|
C | G | 1 | a0002c0001t0002g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6026-29C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/27 | chr17 | 81460501 | ||||||
chr17:81460768
|
C | G | 51 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(48): Show | 51 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.6202+62C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460768 | ||||||
chr17:81460796
|
C | T | 175 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(172): Show | 178 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.6203-70C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460796 | ||||||
chr17:81460823
|
G | A | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6203-43G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460823 | ||||||
chr17:81460859
|
C | G | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.6203-7C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460859 | ||||||
chr17:81462054
|
C | T | 2 | a0001c0009t0030g0263a0001c0009t0037g0319 | 2 | HG02055.hp1 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.7383+8C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462054 | ||||||
chr17:81462202
|
A | G | 149 | a0001c0010t0001g0034a0001c0010t0001g0082a0001c0010t0001g0255others(146): Show | 152 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.7383+156A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462202 | ||||||
chr17:81462204
|
G | A | 3 | a0003c0002t0004g0170a0003c0002t0004g0171a0003c0002t0004g0172 | 3 | HG01167.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.7383+158G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462204 | ||||||
chr17:81462221
|
G | A | 4 | a0009c0013t0006g0029a0009c0013t0006g0072a0009c0013t0006g0140others(1): Show | 4 | HG01192.hp2 HG01516.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.7383+175G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462221 | ||||||
chr17:81462227
|
G | A | 1 | a0002c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.7383+181G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462227 | ||||||
chr17:81462239
|
C | T | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7383+193C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462239 | ||||||
chr17:81462292
|
T | C | 326 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(323): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.7383+246T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462292 | ||||||
chr17:81462332
|
T | C | 278 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(275): Show | 281 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.7383+286T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462332 | ||||||
chr17:81462382
|
C | G | 25 | a0001c0012t0002g0058a0001c0012t0002g0112a0001c0012t0002g0133others(22): Show | 25 | HG00099.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.7383+336C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462382 | ||||||
chr17:81462423
|
T | C | 3 | a0017c0023t0015g0277a0017c0023t0038g0027a0018c0106t0010g0328 | 3 | HG02486.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.7384-317T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462423 | ||||||
chr17:81462462
|
T | A | 1 | a0002c0001t0001g0109 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.7384-278T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462462 | ||||||
chr17:81462463
|
G | C | 2 | a0001c0007t0016g0234a0001c0007t0033g0135 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.7384-277G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462463 | ||||||
chr17:81462502
|
A | G | 1 | a0001c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7384-238A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462502 | ||||||
chr17:81462512
|
C | T | 1 | a0039c0058t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7384-228C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462512 | ||||||
chr17:81462549
|
C | G | 50 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(47): Show | 50 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.7384-191C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462549 | ||||||
chr17:81462576
|
G | A | 7 | a0001c0009t0006g0134a0002c0001t0006g0148a0009c0013t0006g0029others(4): Show | 7 | HG01192.hp2 HG01261.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.7384-164G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462576 | ||||||
chr17:81462597
|
G | A | 1 | a0039c0058t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7384-143G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462597 | ||||||
chr17:81462624
|
A | T | 3 | a0001c0021t0002g0077a0001c0021t0002g0114a0035c0095t0002g0146 | 3 | HG00099.hp2 HG00733.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.7384-116A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462624 | ||||||
chr17:81462685
|
C | T | 173 | a0001c0003t0003g0044a0001c0003t0003g0046a0001c0003t0003g0047others(170): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.7384-55C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462685 | ||||||
chr17:81463009
|
C | T | 25 | a0001c0012t0002g0058a0001c0012t0002g0112a0001c0012t0002g0133others(22): Show | 25 | HG00099.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.7620+33C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463009 | ||||||
chr17:81463090
|
C | T | 3 | a0003c0002t0001g0049a0008c0024t0001g0175a0008c0024t0001g0306 | 3 | HG03831.hp2 HG04204.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.7620+114C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463090 | ||||||
chr17:81463106
|
C | T | 1 | a0007c0008t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7620+130C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463106 | ||||||
chr17:81463132
|
A | C | 4 | a0004c0011t0002g0120a0004c0011t0002g0162a0004c0011t0004g0071others(1): Show | 4 | HG01074.hp1 HG02735.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.7620+156A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463132 | ||||||
chr17:81463175
|
T | C | 3 | a0003c0018t0002g0210a0004c0004t0002g0092a0004c0004t0002g0093 | 3 | HG00733.hp2 HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.7620+199T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463175 | ||||||
chr17:81463230
|
G | A | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7620+254G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463230 | ||||||
chr17:81463359
|
C | T | 1 | a0001c0003t0003g0048 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7621-252C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463359 | ||||||
chr17:81463369
|
G | A | 2 | a0001c0007t0016g0234a0001c0007t0033g0135 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.7621-242G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463369 | ||||||
chr17:81463529
|
G | A | 1 | a0001c0007t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7621-82G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463529 | ||||||
chr17:81463530
|
G | GTGGGCGG others(15): Show |
1 | a0001c0003t0003g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7621-75_7621-54dup others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr17 | 81463530 | |||||
chr17:81463535
|
C | T | 1 | a0001c0003t0003g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7621-76C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463535 |