geneid | 54928 |
---|---|
ensemblid | ENSG00000104331.9 |
hgncid | 26019 |
symbol | BPNT2 |
name | 3'(2'), 5'-bisphosphate nucleotidase 2 |
refseq_nuc | NM_017813.5 |
refseq_prot | NP_060283.3 |
ensembl_nuc | ENST00000262644.9 |
ensembl_prot | ENSP00000262644.4 |
mane_status | MANE Select |
chr | chr8 |
start | 56957931 |
end | 56993867 |
strand | - |
ver | v1.2 |
region | chr8:56957931-56993867 |
region5000 | chr8:56952931-56998867 |
regionname0 | BPNT2_chr8_56957931_56993867 |
regionname5000 | BPNT2_chr8_56952931_56998867 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 359 | 352 | 75 | 55 | 172 | 10 | 38 | 134 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0002 | 0/0 | 359 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0003 | 0/0 | 359 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0004 | 0/0 | 359 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0005 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1080 | 349 | 72 | 55 | 172 | 10 | 38 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
c0002 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
c0003 | 0/0 | 1080 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
c0004 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
c0005 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
c0006 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 6145 | 143 | 36 | 25 | 59 | 8 | 14 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0002 | 0/0 | 6145 | 54 | 6 | 9 | 32 | 1 | 6 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0003 | 0/0 | 6145 | 53 | 0 | 2 | 44 | 1 | 6 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0004 | 1/0 | 6145 | 41 | 7 | 4 | 22 | 0 | 7 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0005 | 0/0 | 6145 | 6 | 0 | 6 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0006 | 0/0 | 6138 | 5 | 4 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0007 | 0/0 | 6145 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0008 | 0/0 | 6144 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0009 | 0/0 | 6145 | 4 | 4 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0010 | 0/0 | 6145 | 4 | 4 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0011 | 0/0 | 6145 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0012 | 0/0 | 6145 | 3 | 0 | 0 | 0 | 1 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0013 | 0/0 | 6145 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0014 | 0/0 | 6141 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0015 | 0/0 | 6145 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0016 | 0/0 | 6145 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0017 | 0/0 | 6145 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0018 | 0/0 | 6145 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0019 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0020 | 0/0 | 6145 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0021 | 0/0 | 6145 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0022 | 0/0 | 6145 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0023 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0024 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0025 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0026 | 0/0 | 6145 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0027 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0028 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0029 | 0/0 | 6145 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0030 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0031 | 0/0 | 6145 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0032 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0033 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0034 | 0/0 | 6145 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0035 | 0/0 | 6145 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0036 | 0/0 | 6145 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
t0037 | 0/0 | 6145 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0002 | 0/1 | 10 | 0 | 1 | 7 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0003 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0004 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0005 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0006 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0008 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0011 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1080 | 349 | 72 | 55 | 172 | 10 | 38 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0002 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0002c0003 | 0/0 | 1080 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0003c0006 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0004c0005 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0005c0004 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7224 | 142 | 36 | 24 | 59 | 8 | 14 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0002 | 0/0 | 7224 | 53 | 6 | 9 | 32 | 0 | 6 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0003 | 0/0 | 7224 | 52 | 0 | 2 | 44 | 0 | 6 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0004 | 1/0 | 7224 | 41 | 7 | 4 | 22 | 0 | 7 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0005 | 0/0 | 7224 | 6 | 0 | 6 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0006 | 0/0 | 7217 | 5 | 4 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0007 | 0/0 | 7224 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0008 | 0/0 | 7223 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0009 | 0/0 | 7224 | 4 | 4 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0010 | 0/0 | 7224 | 4 | 4 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0011 | 0/0 | 7224 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0012 | 0/0 | 7224 | 3 | 0 | 0 | 0 | 1 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0013 | 0/0 | 7224 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0014 | 0/0 | 7220 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0015 | 0/0 | 7224 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0016 | 0/0 | 7224 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0017 | 0/0 | 7224 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0018 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0019 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0020 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0021 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0022 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0023 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0026 | 0/0 | 7224 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0027 | 0/0 | 7223 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0028 | 0/0 | 7223 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0029 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0030 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0031 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0032 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0033 | 0/0 | 7223 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0034 | 0/0 | 7224 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0035 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0001t0036 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0002t0024 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0002t0025 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0001c0002t0037 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0002c0003t0001 | 0/0 | 7224 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0003c0006t0003 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0004c0005t0002 | 0/0 | 7224 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
a0005c0004t0013 | 0/0 | 7224 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | copy fasta | chr8 | 56952931 | 56998867 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/1 | 10 | 0 | 1 | 7 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0005 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0008 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0003 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0006 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0004 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0005g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0005g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0007g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0008g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0011g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0011g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0012g0011 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0014g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0015g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0016g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0017g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0018g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0019g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0020g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0021g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0022g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0023g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0026g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0027g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0028g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0029g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0030g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0031g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0032g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0033g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0034g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0035g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0001t0036g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0002t0024g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0002t0025g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0001c0002t0037g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0003c0006t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0004c0005t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
a0005c0004t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00323 | hp1 | a0004 | c0005 | t0002 | g0199 | EUR | FIN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00621 | hp2 | a0001 | c0001 | t0017 | g0120 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00738 | hp1 | a0001 | c0001 | t0018 | g0130 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0185 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01070 | hp2 | a0001 | c0001 | t0014 | g0038 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01071 | hp2 | a0001 | c0001 | t0014 | g0038 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01081 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01099 | hp2 | a0001 | c0001 | t0022 | g0078 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01175 | hp1 | a0001 | c0001 | t0029 | g0179 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0071 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01358 | hp1 | a0001 | c0001 | t0036 | g0257 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01516 | hp2 | a0003 | c0006 | t0003 | g0251 | EUR | IBS | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01952 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02040 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02055 | hp2 | a0001 | c0002 | t0024 | g0182 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02145 | hp2 | a0001 | c0001 | t0016 | g0190 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0256 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02258 | hp1 | a0001 | c0001 | t0016 | g0198 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0043 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02300 | hp2 | a0001 | c0001 | t0011 | g0108 | AMR | PEL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02451 | hp1 | a0001 | c0002 | t0037 | g0259 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0211 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02717 | hp2 | a0001 | c0001 | t0033 | g0045 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02723 | hp2 | a0005 | c0004 | t0013 | g0189 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02886 | hp1 | a0001 | c0001 | t0030 | g0188 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02922 | hp2 | a0001 | c0001 | t0032 | g0088 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02976 | hp1 | a0001 | c0001 | t0019 | g0178 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03041 | hp2 | a0001 | c0001 | t0028 | g0046 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0204 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0089 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03486 | hp2 | a0001 | c0002 | t0025 | g0183 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03579 | hp1 | a0001 | c0001 | t0023 | g0138 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03669 | hp2 | a0001 | c0001 | t0012 | g0011 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03704 | hp1 | a0001 | c0001 | t0012 | g0011 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03942 | hp1 | a0001 | c0001 | t0035 | g0197 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0062 | SAS | BEB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG04115 | hp2 | a0001 | c0001 | t0021 | g0124 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | STU | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | CHB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18939 | hp2 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18942 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18965 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18971 | hp2 | a0001 | c0001 | t0015 | g0135 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18980 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18990 | hp1 | a0001 | c0001 | t0015 | g0139 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18992 | hp1 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18998 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19003 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19055 | hp1 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19083 | hp2 | a0001 | c0001 | t0034 | g0195 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19088 | hp1 | a0001 | c0001 | t0026 | g0123 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ASW | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ASW | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20752 | hp2 | a0001 | c0001 | t0012 | g0011 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20805 | hp2 | a0001 | c0001 | t0020 | g0127 | EUR | TSI | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | GIH | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20905 | hp2 | a0001 | c0001 | t0031 | g0146 | SAS | GIH | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02109 | hp1 | a0001 | c0001 | t0027 | g0044 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0181 | AFR | ACB | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | USA | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | LWK | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0067 | REF | REF | BPNT2_chr8_56952931_56998867 | BPNT2 | chr8 | 56952931 | 56998867 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:56963909
|
C | T | 1 | a0004 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.964G>A | p.Glu322Lys | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1246/7224 | 964/1080 | 322/359 | chr8 | 56963909 | ||
chr8:56964017
|
T | C | 1 | a0003 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.856A>G | p.Lys286Glu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1138/7224 | 856/1080 | 286/359 | chr8 | 56964017 | ||
chr8:56993326
|
C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.260G>C | p.Ser87Thr | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 542/7224 | 260/1080 | 87/359 | chr8 | 56993326 | ||
chr8:56993329
|
T | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.257A>G | p.Glu86Gly | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 539/7224 | 257/1080 | 86/359 | chr8 | 56993329 | ||
chr8:56993330
|
C | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.256G>A | p.Glu86Lys | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 538/7224 | 256/1080 | 86/359 | chr8 | 56993330 | ||
chr8:56993338
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.248G>T | p.Arg83Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 530/7224 | 248/1080 | 83/359 | chr8 | 56993338 | ||
chr8:56993341
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.245G>T | p.Arg82Met | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 527/7224 | 245/1080 | 82/359 | chr8 | 56993341 | ||
chr8:56993342
|
T | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.244A>T | p.Arg82Trp | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 526/7224 | 244/1080 | 82/359 | chr8 | 56993342 | ||
chr8:56993344
|
A | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.242T>A | p.Val81Glu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 524/7224 | 242/1080 | 81/359 | chr8 | 56993344 | ||
chr8:56993347
|
T | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.239A>T | p.Glu80Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 521/7224 | 239/1080 | 80/359 | chr8 | 56993347 | ||
chr8:56993348
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | stop_gained | HIGH | c.238G>T | p.Glu80* | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 520/7224 | 238/1080 | 80/359 | chr8 | 56993348 | ||
chr8:56993350
|
T | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.236A>C | p.Asp79Ala | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 518/7224 | 236/1080 | 79/359 | chr8 | 56993350 | ||
chr8:56993351
|
C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.235G>C | p.Asp79His | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 517/7224 | 235/1080 | 79/359 | chr8 | 56993351 | ||
chr8:56993353
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.233G>T | p.Gly78Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 515/7224 | 233/1080 | 78/359 | chr8 | 56993353 | ||
chr8:56993354
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.232G>T | p.Gly78Cys | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 514/7224 | 232/1080 | 78/359 | chr8 | 56993354 | ||
chr8:56993356
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.230G>T | p.Gly77Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 512/7224 | 230/1080 | 77/359 | chr8 | 56993356 | ||
chr8:56993363
|
C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.223G>C | p.Val75Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 505/7224 | 223/1080 | 75/359 | chr8 | 56993363 | ||
chr8:56993366
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.220G>T | p.Ala74Ser | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 502/7224 | 220/1080 | 74/359 | chr8 | 56993366 | ||
chr8:56993368
|
G | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.218C>G | p.Ala73Gly | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 500/7224 | 218/1080 | 73/359 | chr8 | 56993368 | ||
chr8:56993388
|
C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.198G>C | p.Met66Ile | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 480/7224 | 198/1080 | 66/359 | chr8 | 56993388 | ||
chr8:56993389
|
A | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.197T>G | p.Met66Arg | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 479/7224 | 197/1080 | 66/359 | chr8 | 56993389 | ||
chr8:56993390
|
T | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.196A>C | p.Met66Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 478/7224 | 196/1080 | 66/359 | chr8 | 56993390 | ||
chr8:56993391
|
C | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.195G>T | p.Glu65Asp | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 477/7224 | 195/1080 | 65/359 | chr8 | 56993391 | ||
chr8:56993396
|
G | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.190C>A | p.Arg64Ser | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 472/7224 | 190/1080 | 64/359 | chr8 | 56993396 | ||
chr8:56993397
|
C | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.189G>C | p.Leu63Phe | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 471/7224 | 189/1080 | 63/359 | chr8 | 56993397 | ||
chr8:56993398
|
A | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.188T>G | p.Leu63Trp | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 470/7224 | 188/1080 | 63/359 | chr8 | 56993398 | ||
chr8:56993399
|
A | T | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.187T>A | p.Leu63Met | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 469/7224 | 187/1080 | 63/359 | chr8 | 56993399 | ||
chr8:56993413
|
C | G | 1 | a0002 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.173G>C | p.Gly58Ala | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 455/7224 | 173/1080 | 58/359 | chr8 | 56993413 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:56963934
|
C | T | 1 | a0001c0002 | 3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.939G>A | p.Gly313Gly | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1221/7224 | 939/1080 | 313/359 | chr8 | 56963934 | ||
chr8:56993331
|
G | C | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.255C>G | p.Arg85Arg | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 537/7224 | 255/1080 | 85/359 | chr8 | 56993331 | ||
chr8:56993343
|
C | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.243G>C | p.Val81Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 525/7224 | 243/1080 | 81/359 | chr8 | 56993343 | ||
chr8:56993364
|
T | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.222A>C | p.Ala74Ala | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 504/7224 | 222/1080 | 74/359 | chr8 | 56993364 | ||
chr8:56993370
|
C | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.216G>C | p.Leu72Leu | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 498/7224 | 216/1080 | 72/359 | chr8 | 56993370 | ||
chr8:56993373
|
C | G | 1 | a0005c0004 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.213G>C | p.Val71Val | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 495/7224 | 213/1080 | 71/359 | chr8 | 56993373 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:56958063
|
T | C | 3 | a0001c0001t0005a0001c0001t0007a0001c0001t0036 | 12 | HG01074.hp1 HG01168.hp1 HG01358.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5730A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5730 | chr8 | 56958063 | |||||
chr8:56958159
|
T | C | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5634A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5634 | chr8 | 56958159 | |||||
chr8:56958281
|
A | G | 3 | a0001c0001t0006a0001c0001t0027a0001c0001t0033 | 7 | HG00741.hp1 HG02109.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5512T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5512 | chr8 | 56958281 | |||||
chr8:56958288
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*5505A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5505 | chr8 | 56958288 | |||||
chr8:56958301
|
C | T | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5492G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5492 | chr8 | 56958301 | |||||
chr8:56958491
|
G | A | 2 | a0001c0001t0028a0001c0002t0024 | 2 | HG02055.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5302C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5302 | chr8 | 56958491 | |||||
chr8:56958659
|
T | C | 1 | a0001c0001t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5134A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5134 | chr8 | 56958659 | |||||
chr8:56958779
|
T | C | 8 | a0001c0001t0009a0001c0001t0014a0001c0001t0027others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5014A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 5014 | chr8 | 56958779 | |||||
chr8:56958903
|
G | A | 6 | a0001c0001t0002a0001c0001t0013a0001c0001t0016others(3): Show | 60 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4890C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4890 | chr8 | 56958903 | |||||
chr8:56959134
|
A | G | 1 | a0001c0001t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4659T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4659 | chr8 | 56959134 | |||||
chr8:56959363
|
T | C | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4430A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4430 | chr8 | 56959363 | |||||
chr8:56959478
|
G | A | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4315C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4315 | chr8 | 56959478 | |||||
chr8:56959529
|
C | T | 1 | a0001c0001t0020 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4264G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4264 | chr8 | 56959529 | |||||
chr8:56959584
|
C | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4209G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4209 | chr8 | 56959584 | |||||
chr8:56959667
|
AGAT | A | 1 | a0001c0001t0006 | 5 | HG00741.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4123_*4125delATC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 4123 | chr8 | 56959667 | |||||
chr8:56959836
|
G | T | 1 | a0001c0002t0024 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3957C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3957 | chr8 | 56959836 | |||||
chr8:56959882
|
C | T | 1 | a0001c0001t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3911G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3911 | chr8 | 56959882 | |||||
chr8:56960062
|
A | C | 1 | a0001c0001t0015 | 2 | NA18971.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3731 | chr8 | 56960062 | |||||
chr8:56960120
|
T | C | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*3673A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3673 | chr8 | 56960120 | |||||
chr8:56960492
|
T | A | 1 | a0001c0001t0022 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3301A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3301 | chr8 | 56960492 | |||||
chr8:56960589
|
T | C | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0029others(2): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3204A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3204 | chr8 | 56960589 | |||||
chr8:56960715
|
A | C | 1 | a0001c0001t0032 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3078T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3078 | chr8 | 56960715 | |||||
chr8:56960715
|
AT | A | 1 | a0001c0001t0008 | 5 | NA18939.hp2 NA18965.hp1 NA18980.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3077delA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 3077 | chr8 | 56960715 | |||||
chr8:56960848
|
T | C | 1 | a0001c0001t0023 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2945A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2945 | chr8 | 56960848 | |||||
chr8:56960930
|
A | G | 1 | a0001c0001t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2863T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2863 | chr8 | 56960930 | |||||
chr8:56961162
|
T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2631A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2631 | chr8 | 56961162 | |||||
chr8:56961185
|
T | G | 1 | a0001c0001t0012 | 3 | HG03669.hp2 HG03704.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2608A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2608 | chr8 | 56961185 | |||||
chr8:56961285
|
A | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2508T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2508 | chr8 | 56961285 | |||||
chr8:56961411
|
T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2382A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2382 | chr8 | 56961411 | |||||
chr8:56961505
|
C | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2288G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2288 | chr8 | 56961505 | |||||
chr8:56961644
|
C | A | 3 | a0001c0002t0024a0001c0002t0025a0001c0002t0037 | 3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2149G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 2149 | chr8 | 56961644 | |||||
chr8:56961796
|
C | T | 1 | a0001c0001t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1997G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1997 | chr8 | 56961796 | |||||
chr8:56961840
|
C | T | 1 | a0001c0001t0035 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1953 | chr8 | 56961840 | |||||
chr8:56962142
|
C | T | 1 | a0001c0001t0018 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1651G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1651 | chr8 | 56962142 | |||||
chr8:56962195
|
G | A | 1 | a0001c0001t0026 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1598C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1598 | chr8 | 56962195 | |||||
chr8:56962300
|
A | G | 1 | a0001c0001t0036 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1493 | chr8 | 56962300 | |||||
chr8:56962479
|
CG | C | 3 | a0001c0001t0027a0001c0001t0028a0001c0001t0033 | 3 | HG02109.hp1 HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1313delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 1313 | chr8 | 56962479 | |||||
chr8:56962812
|
TA | T | 2 | a0001c0001t0006a0001c0001t0014 | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*980delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 980 | chr8 | 56962812 | |||||
chr8:56962926
|
A | G | 1 | a0001c0001t0017 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 867 | chr8 | 56962926 | |||||
chr8:56963011
|
C | T | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0029others(2): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 782 | chr8 | 56963011 | |||||
chr8:56963029
|
G | A | 4 | a0001c0001t0002a0001c0001t0016a0001c0001t0035others(1): Show | 57 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 764 | chr8 | 56963029 | |||||
chr8:56963092
|
G | A | 6 | a0001c0001t0003a0001c0001t0005a0001c0001t0029others(3): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*701C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 701 | chr8 | 56963092 | |||||
chr8:56963240
|
T | C | 1 | a0001c0001t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 553 | chr8 | 56963240 | |||||
chr8:56963286
|
TACA | T | 2 | a0001c0001t0006a0001c0001t0014 | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*506delTGT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 504 | chr8 | 56963286 | |||||
chr8:56963435
|
C | T | 1 | a0001c0001t0011 | 3 | HG01081.hp2 HG01952.hp2 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*358G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 358 | chr8 | 56963435 | |||||
chr8:56963646
|
G | A | 2 | a0001c0001t0010a0001c0001t0032 | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 147 | chr8 | 56963646 | |||||
chr8:56963708
|
T | C | 1 | a0001c0001t0033 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 5/5 | 85 | chr8 | 56963708 | |||||
chr8:56993710
|
G | A | 7 | a0001c0001t0002a0001c0001t0013a0001c0001t0016others(4): Show | 61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-125C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | chr8 | 56993710 | ||||||
chr8:56993754
|
G | A | 4 | a0001c0001t0003a0001c0001t0005a0001c0001t0036others(1): Show | 60 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-169C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 169 | chr8 | 56993754 | |||||
chr8:56993848
|
T | C | 1 | a0001c0002t0037 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-263A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/5 | 263 | chr8 | 56993848 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:56964123
|
C | G | 1 | a0001c0001t0003g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.809-59G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964123 | ||||||
chr8:56964163
|
T | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0225 | 2 | HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.809-99A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964163 | ||||||
chr8:56964340
|
T | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.809-276A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964340 | ||||||
chr8:56964359
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.809-295G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964359 | ||||||
chr8:56964414
|
C | T | 3 | a0001c0001t0027g0044a0001c0001t0028g0046a0001c0001t0033g0045 | 3 | HG02109.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.809-350G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964414 | ||||||
chr8:56964448
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.809-384C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964448 | ||||||
chr8:56964469
|
T | TTTTTGTA | 5 | a0001c0001t0001g0093a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG02040.hp1 HG02080.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-412_809-406dup others(7): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964469 | ||||||
chr8:56964483
|
A | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0145a0001c0001t0001g0156others(3): Show | 7 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-419T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964483 | ||||||
chr8:56964527
|
T | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0167a0001c0001t0001g0177 | 4 | HG01109.hp2 HG02055.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-463A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964527 | ||||||
chr8:56964551
|
T | C | 1 | a0001c0001t0004g0054 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.809-487A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964551 | ||||||
chr8:56964567
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.809-503G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964567 | ||||||
chr8:56964581
|
G | A | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.809-517C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964581 | ||||||
chr8:56964675
|
T | C | 1 | a0001c0001t0033g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.809-611A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964675 | ||||||
chr8:56964703
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.809-639A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964703 | ||||||
chr8:56964710
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.809-646G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964710 | ||||||
chr8:56964774
|
C | T | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.809-710G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964774 | ||||||
chr8:56964775
|
G | A | 1 | a0001c0001t0004g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.809-711C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56964775 | ||||||
chr8:56965058
|
G | A | 36 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.809-994C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965058 | ||||||
chr8:56965115
|
C | T | 1 | a0001c0001t0022g0078 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.809-1051G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965115 | ||||||
chr8:56965136
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0243 | 3 | HG02135.hp2 HG02523.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.808+1055C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965136 | ||||||
chr8:56965260
|
G | A | 3 | a0001c0001t0003g0231a0001c0001t0003g0237a0001c0001t0003g0240 | 3 | NA18941.hp2 NA18947.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.808+931C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965260 | ||||||
chr8:56965275
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808+916G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965275 | ||||||
chr8:56965514
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.808+677A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965514 | ||||||
chr8:56965557
|
T | C | 1 | a0001c0001t0004g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.808+634A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965557 | ||||||
chr8:56965697
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.808+494G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965697 | ||||||
chr8:56965755
|
T | C | 48 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(45): Show | 62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.808+436A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965755 | ||||||
chr8:56965818
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.808+373G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965818 | ||||||
chr8:56965878
|
C | T | 48 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(45): Show | 62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.808+313G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56965878 | ||||||
chr8:56966040
|
G | T | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.808+151C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56966040 | ||||||
chr8:56966148
|
G | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0148others(2): Show | 6 | NA18948.hp1 NA18977.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.808+43C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 4/4 | chr8 | 56966148 | ||||||
chr8:56966431
|
T | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-79A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966431 | ||||||
chr8:56966724
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.647-372G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966724 | ||||||
chr8:56966879
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.647-527A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966879 | ||||||
chr8:56966999
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.647-647A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56966999 | ||||||
chr8:56967096
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.647-744C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967096 | ||||||
chr8:56967262
|
T | C | 1 | a0001c0001t0030g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.647-910A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967262 | ||||||
chr8:56967418
|
A | G | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.647-1066T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967418 | ||||||
chr8:56967456
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.647-1104G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967456 | ||||||
chr8:56967634
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.647-1282G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967634 | ||||||
chr8:56967784
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0031g0146 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.647-1432C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967784 | ||||||
chr8:56967895
|
C | T | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.647-1543G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56967895 | ||||||
chr8:56968210
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.647-1858A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968210 | ||||||
chr8:56968300
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.647-1948A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968300 | ||||||
chr8:56968305
|
A | C | 1 | a0001c0001t0006g0185 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.647-1953T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968305 | ||||||
chr8:56968306
|
A | G | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.647-1954T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968306 | ||||||
chr8:56968344
|
G | A | 1 | a0001c0001t0026g0123 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.647-1992C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968344 | ||||||
chr8:56968389
|
T | TA | 42 | a0001c0001t0001g0136a0001c0001t0003g0001a0001c0001t0003g0006others(39): Show | 67 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.647-2038dupT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968389 | ||||||
chr8:56968399
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.647-2047T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968399 | ||||||
chr8:56968651
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.647-2299G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968651 | ||||||
chr8:56968695
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.647-2343C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56968695 | ||||||
chr8:56969362
|
C | G | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-3010G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969362 | ||||||
chr8:56969362
|
C | T | 1 | a0001c0001t0010g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.647-3010G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969362 | ||||||
chr8:56969374
|
T | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0150a0001c0001t0026g0123 | 3 | NA18962.hp2 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.647-3022A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969374 | ||||||
chr8:56969514
|
C | G | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-3162G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969514 | ||||||
chr8:56969514
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.647-3162G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969514 | ||||||
chr8:56969520
|
T | A | 36 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.647-3168A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969520 | ||||||
chr8:56969585
|
CA | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-3234delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969585 | ||||||
chr8:56969627
|
G | A | 1 | a0001c0001t0004g0071 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647-3275C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969627 | ||||||
chr8:56969748
|
C | T | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.647-3396G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969748 | ||||||
chr8:56969897
|
T | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0077others(19): Show | 25 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.647-3545A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56969897 | ||||||
chr8:56970015
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.647-3663G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970015 | ||||||
chr8:56970768
|
T | C | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.647-4416A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970768 | ||||||
chr8:56970862
|
C | T | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-4510G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970862 | ||||||
chr8:56970863
|
G | A | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.647-4511C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970863 | ||||||
chr8:56970878
|
TTCATAAA others(33): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.647-4566_647-4527d others(42): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56970878 | ||||||
chr8:56971269
|
TA | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0004g0061others(4): Show | 7 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.647-4918delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971269 | ||||||
chr8:56971269
|
TAA | T | 78 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(75): Show | 117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.647-4919_647-4918d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971269 | ||||||
chr8:56971305
|
A | G | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.647-4953T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971305 | ||||||
chr8:56971321
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.647-4969G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971321 | ||||||
chr8:56971380
|
G | T | 2 | a0001c0001t0004g0048a0001c0001t0004g0052 | 2 | HG00423.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.647-5028C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971380 | ||||||
chr8:56971422
|
T | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0105 | 2 | HG01167.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.647-5070A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971422 | ||||||
chr8:56971504
|
T | A | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.647-5152A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971504 | ||||||
chr8:56971600
|
G | A | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.647-5248C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971600 | ||||||
chr8:56971619
|
T | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.647-5267A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971619 | ||||||
chr8:56971649
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.647-5297G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971649 | ||||||
chr8:56971782
|
A | AC | 80 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0027others(77): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.647-5431dupG | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | ||||||
chr8:56971782
|
A | ACC | 53 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0028others(50): Show | 67 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.647-5432_647-5431d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | ||||||
chr8:56971782
|
A | ACCC | 40 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0025others(37): Show | 58 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.647-5433_647-5431d others(5): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | ||||||
chr8:56971782
|
A | ACCCC | 27 | a0001c0001t0001g0007a0001c0001t0001g0125a0001c0001t0001g0131others(24): Show | 31 | HG00323.hp1 HG00597.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.647-5434_647-5431d others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | ||||||
chr8:56971782
|
A | ACCCCC | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0152others(14): Show | 20 | HG00741.hp2 HG01071.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.647-5435_647-5431d others(7): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971782 | ||||||
chr8:56971784
|
C | CA | 4 | a0001c0001t0010g0087a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-5433_647-5432i others(3): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971784 | ||||||
chr8:56971852
|
T | C | 1 | a0001c0001t0030g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.647-5500A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971852 | ||||||
chr8:56971935
|
A | C | 1 | a0001c0001t0020g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.647-5583T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56971935 | ||||||
chr8:56972036
|
AG | A | 47 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(44): Show | 61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.647-5685delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972036 | ||||||
chr8:56972154
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0028g0046 | 3 | HG03041.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.647-5802C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972154 | ||||||
chr8:56972171
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.647-5819C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972171 | ||||||
chr8:56972184
|
C | A | 6 | a0001c0001t0003g0232a0001c0001t0003g0234a0001c0001t0003g0235others(3): Show | 6 | HG01123.hp1 NA18965.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.647-5832G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972184 | ||||||
chr8:56972423
|
A | G | 3 | a0001c0001t0002g0215a0001c0001t0002g0217a0001c0001t0002g0226 | 3 | HG02451.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.646+5627T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972423 | ||||||
chr8:56972433
|
G | A | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+5617C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972433 | ||||||
chr8:56972505
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.646+5545A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972505 | ||||||
chr8:56972512
|
T | A | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646+5538A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972512 | ||||||
chr8:56972528
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.646+5522G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972528 | ||||||
chr8:56972565
|
C | T | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+5485G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972565 | ||||||
chr8:56972577
|
TA | T | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.646+5472delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972577 | ||||||
chr8:56972842
|
T | C | 6 | a0001c0001t0006g0174a0001c0001t0006g0181a0001c0001t0006g0184others(3): Show | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.646+5208A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972842 | ||||||
chr8:56972864
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.646+5186A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56972864 | ||||||
chr8:56973018
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.646+5032C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973018 | ||||||
chr8:56973106
|
G | A | 1 | a0001c0001t0015g0139 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.646+4944C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973106 | ||||||
chr8:56973114
|
T | TCCACTGA others(33): Show |
1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.646+4896_646+4935d others(42): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973114 | ||||||
chr8:56973154
|
C | T | 44 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(41): Show | 58 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.646+4896G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973154 | ||||||
chr8:56973162
|
G | C | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.646+4888C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973162 | ||||||
chr8:56973366
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.646+4684T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973366 | ||||||
chr8:56973403
|
G | T | 3 | a0001c0001t0006g0174a0001c0001t0006g0185a0001c0001t0006g0186 | 3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.646+4647C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973403 | ||||||
chr8:56973475
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.646+4575G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973475 | ||||||
chr8:56973486
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02559.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.646+4564A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973486 | ||||||
chr8:56973657
|
T | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+4393A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973657 | ||||||
chr8:56973666
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0119 | 2 | HG00621.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.646+4384T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973666 | ||||||
chr8:56973674
|
T | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.646+4376A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973674 | ||||||
chr8:56973686
|
C | T | 1 | a0001c0001t0021g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646+4364G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973686 | ||||||
chr8:56973688
|
A | G | 1 | a0001c0001t0006g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.646+4362T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973688 | ||||||
chr8:56973865
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.646+4185T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56973865 | ||||||
chr8:56974004
|
C | G | 2 | a0001c0001t0016g0190a0001c0001t0016g0198 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.646+4046G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974004 | ||||||
chr8:56974238
|
T | C | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+3812A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974238 | ||||||
chr8:56974385
|
T | TTCAAAC | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+3664_646+3665i others(8): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974385 | ||||||
chr8:56974564
|
C | T | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+3486G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974564 | ||||||
chr8:56974659
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0151 | 2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.646+3391C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974659 | ||||||
chr8:56974746
|
G | T | 9 | a0001c0001t0002g0014a0001c0001t0002g0039a0001c0001t0002g0214others(6): Show | 12 | HG00673.hp1 HG01074.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.646+3304C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974746 | ||||||
chr8:56974762
|
A | G | 1 | a0001c0001t0030g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.646+3288T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974762 | ||||||
chr8:56974820
|
A | T | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+3230T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56974820 | ||||||
chr8:56975002
|
G | A | 1 | a0001c0001t0003g0253 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.646+3048C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975002 | ||||||
chr8:56975186
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.646+2864G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975186 | ||||||
chr8:56975289
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 88 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.646+2761C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975289 | ||||||
chr8:56975305
|
T | C | 2 | a0001c0001t0004g0062a0001c0001t0004g0076 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.646+2745A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975305 | ||||||
chr8:56975474
|
A | T | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646+2576T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975474 | ||||||
chr8:56975884
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.646+2166C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56975884 | ||||||
chr8:56976042
|
A | G | 1 | a0001c0001t0007g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.646+2008T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976042 | ||||||
chr8:56976299
|
T | C | 1 | a0001c0001t0004g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.646+1751A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976299 | ||||||
chr8:56976706
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0145a0001c0001t0001g0169 | 4 | HG02647.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+1344C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976706 | ||||||
chr8:56976850
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.646+1200A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56976850 | ||||||
chr8:56977104
|
A | G | 11 | a0001c0001t0006g0174a0001c0001t0006g0181a0001c0001t0006g0184others(8): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.646+946T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977104 | ||||||
chr8:56977185
|
T | C | 2 | a0001c0001t0027g0044a0001c0001t0033g0045 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.646+865A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977185 | ||||||
chr8:56977248
|
A | G | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+802T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977248 | ||||||
chr8:56977264
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.646+786C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977264 | ||||||
chr8:56977625
|
GTAC | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0077others(13): Show | 18 | HG01069.hp2 HG01167.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.646+422_646+424del others(3): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977625 | ||||||
chr8:56977631
|
C | T | 16 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0077others(13): Show | 18 | HG01069.hp2 HG01167.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.646+419G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977631 | ||||||
chr8:56977652
|
G | T | 1 | a0001c0001t0001g0012 | 3 | HG00642.hp1 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.646+398C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977652 | ||||||
chr8:56977732
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.646+318A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977732 | ||||||
chr8:56977774
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.646+276T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977774 | ||||||
chr8:56977776
|
TG | T | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.646+273delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977776 | ||||||
chr8:56977790
|
T | C | 1 | a0001c0001t0010g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646+260A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 3/4 | chr8 | 56977790 | ||||||
chr8:56978440
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0145a0001c0001t0001g0169 | 4 | HG02647.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-295C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978440 | ||||||
chr8:56978566
|
C | T | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-421G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978566 | ||||||
chr8:56978664
|
T | TA | 48 | a0001c0001t0001g0163a0001c0001t0002g0003a0001c0001t0002g0013others(45): Show | 62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.551-520dupT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978664 | ||||||
chr8:56978680
|
T | C | 47 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(44): Show | 61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.551-535A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978680 | ||||||
chr8:56978857
|
T | C | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0027g0044others(2): Show | 7 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.551-712A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978857 | ||||||
chr8:56978891
|
G | A | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.551-746C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978891 | ||||||
chr8:56978913
|
G | C | 2 | a0001c0001t0007g0140a0001c0001t0007g0141 | 2 | HG02040.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.551-768C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56978913 | ||||||
chr8:56979003
|
C | T | 5 | a0001c0001t0004g0072a0001c0001t0008g0019a0001c0001t0008g0053others(2): Show | 6 | NA18939.hp2 NA18965.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-858G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979003 | ||||||
chr8:56979007
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.551-862T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979007 | ||||||
chr8:56979041
|
A | G | 2 | a0001c0001t0027g0044a0001c0001t0033g0045 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.551-896T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979041 | ||||||
chr8:56979355
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.550+680A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979355 | ||||||
chr8:56979404
|
T | C | 3 | a0001c0001t0006g0174a0001c0001t0006g0185a0001c0001t0006g0186 | 3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.550+631A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979404 | ||||||
chr8:56979496
|
T | C | 1 | a0001c0001t0006g0184 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550+539A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979496 | ||||||
chr8:56979679
|
T | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0145a0001c0001t0001g0156others(3): Show | 7 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+356A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979679 | ||||||
chr8:56979706
|
T | C | 1 | a0001c0001t0004g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.550+329A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979706 | ||||||
chr8:56979959
|
A | G | 36 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.550+76T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 2/4 | chr8 | 56979959 | ||||||
chr8:56980235
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.388-38G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980235 | ||||||
chr8:56980533
|
A | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01167.hp2 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.388-336T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980533 | ||||||
chr8:56980534
|
A | G | 1 | a0001c0001t0004g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.388-337T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980534 | ||||||
chr8:56980664
|
G | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(253): Show | 353 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.388-467C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980664 | ||||||
chr8:56980666
|
T | C | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.388-469A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980666 | ||||||
chr8:56980751
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-554A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980751 | ||||||
chr8:56980761
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0180 | 2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.388-564A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980761 | ||||||
chr8:56980819
|
T | C | 1 | a0001c0001t0010g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388-622A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TAC | 9 | a0001c0001t0001g0155a0001c0001t0004g0065a0001c0001t0004g0072others(6): Show | 9 | HG00741.hp1 HG02109.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-624_388-623dup others(2): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACAC | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 7 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-626_388-623dup others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACACAC | 11 | a0001c0001t0001g0037a0001c0001t0001g0077a0001c0001t0001g0092others(8): Show | 14 | HG01167.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.388-628_388-623dup others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0025a0001c0001t0001g0102a0001c0001t0003g0232others(6): Show | 11 | HG01074.hp1 HG01168.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.388-630_388-623dup others(8): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACACACA others(3): Show |
19 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0015others(16): Show | 37 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.388-632_388-623dup others(10): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACACACA others(5): Show |
9 | a0001c0001t0001g0103a0001c0001t0003g0006a0001c0001t0003g0240others(6): Show | 15 | HG01516.hp2 HG02622.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.388-634_388-623dup others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACACACA others(7): Show |
2 | a0001c0001t0003g0241a0001c0001t0003g0254 | 2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.388-636_388-623dup others(14): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TACACACA others(9): Show |
1 | a0001c0001t0002g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.388-638_388-623dup others(16): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TATACAC | 3 | a0001c0001t0002g0200a0001c0001t0002g0208a0001c0001t0002g0213 | 3 | HG00408.hp1 HG00423.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.388-623_388-622ins others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TATACACA others(3): Show |
17 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0039others(14): Show | 29 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-623_388-622ins others(10): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TATACACA others(5): Show |
10 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0203others(7): Show | 10 | HG02080.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-623_388-622ins others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TATACACA others(7): Show |
12 | a0001c0001t0002g0014a0001c0001t0002g0218a0001c0001t0002g0219others(9): Show | 14 | HG00673.hp1 HG01074.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.388-623_388-622ins others(14): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TATACACA others(9): Show |
3 | a0001c0001t0002g0196a0001c0001t0002g0225a0001c0001t0002g0230 | 3 | HG03710.hp2 HG04228.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.388-623_388-622ins others(16): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
T | TATATACA others(5): Show |
1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-623_388-622ins others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
TAC | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 9 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-624_388-623del others(2): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980819
|
TACAC | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(70): Show | 106 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.388-626_388-623del others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980819 | ||||||
chr8:56980821
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.388-624G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980821 | ||||||
chr8:56980852
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0214 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.388-656_388-655ins others(15): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980852 | ||||||
chr8:56980932
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01167.hp2 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.388-735C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56980932 | ||||||
chr8:56981008
|
A | AC | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-812_388-811ins others(1): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981008 | ||||||
chr8:56981029
|
G | C | 1 | a0001c0001t0035g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.388-832C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981029 | ||||||
chr8:56981127
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 343 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.388-930T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981127 | ||||||
chr8:56981177
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.388-980C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981177 | ||||||
chr8:56981324
|
C | T | 47 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(44): Show | 61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1127G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981324 | ||||||
chr8:56981378
|
G | A | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-1181C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981378 | ||||||
chr8:56981407
|
A | C | 1 | a0001c0001t0003g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.388-1210T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981407 | ||||||
chr8:56981636
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0022g0078 | 2 | HG01099.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.388-1439G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981636 | ||||||
chr8:56981800
|
C | A | 1 | a0001c0002t0025g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.388-1603G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981800 | ||||||
chr8:56981901
|
G | A | 1 | a0001c0001t0011g0108 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.388-1704C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981901 | ||||||
chr8:56981917
|
G | A | 1 | a0001c0001t0008g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.388-1720C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981917 | ||||||
chr8:56981944
|
T | C | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0027g0044others(2): Show | 7 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-1747A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56981944 | ||||||
chr8:56982126
|
C | CT | 14 | a0001c0001t0001g0056a0001c0001t0001g0111a0001c0001t0001g0116others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-1930dupA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982126 | ||||||
chr8:56982126
|
C | CTT | 5 | a0001c0001t0006g0174a0001c0001t0006g0181a0001c0001t0006g0185others(2): Show | 6 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-1931_388-1930d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982126 | ||||||
chr8:56982128
|
T | C | 3 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0002g0230 | 3 | NA18969.hp2 NA18986.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.388-1931A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982128 | ||||||
chr8:56982380
|
C | G | 1 | a0001c0001t0030g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.388-2183G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982380 | ||||||
chr8:56982413
|
G | A | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-2216C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982413 | ||||||
chr8:56982510
|
C | T | 5 | a0001c0001t0006g0174a0001c0001t0006g0181a0001c0001t0006g0184others(2): Show | 5 | HG00741.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-2313G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982510 | ||||||
chr8:56982519
|
T | A | 1 | a0001c0001t0002g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.388-2322A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982519 | ||||||
chr8:56982565
|
G | A | 1 | a0001c0001t0006g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.388-2368C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982565 | ||||||
chr8:56982580
|
G | A | 18 | a0001c0001t0003g0009a0001c0001t0003g0231a0001c0001t0003g0232others(15): Show | 24 | HG01074.hp1 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.388-2383C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982580 | ||||||
chr8:56982610
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.388-2413T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982610 | ||||||
chr8:56982642
|
TG | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.388-2446delC | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982642 | ||||||
chr8:56982695
|
T | C | 1 | a0001c0001t0004g0073 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.388-2498A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982695 | ||||||
chr8:56982760
|
T | A | 1 | a0001c0002t0024g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-2563A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982760 | ||||||
chr8:56982872
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-2675A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982872 | ||||||
chr8:56982916
|
C | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 7 | HG01258.hp1 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-2719G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56982916 | ||||||
chr8:56983049
|
C | T | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-2852G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983049 | ||||||
chr8:56983238
|
C | T | 6 | a0001c0001t0006g0174a0001c0001t0006g0185a0001c0001t0006g0186others(3): Show | 6 | HG00741.hp1 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-3041G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983238 | ||||||
chr8:56983542
|
C | T | 2 | a0001c0001t0027g0044a0001c0001t0033g0045 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.388-3345G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983542 | ||||||
chr8:56983659
|
A | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 5 | HG00099.hp2 HG00738.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-3462T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983659 | ||||||
chr8:56983876
|
G | A | 3 | a0001c0001t0006g0174a0001c0001t0006g0185a0001c0001t0006g0186 | 3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.388-3679C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983876 | ||||||
chr8:56983999
|
G | A | 3 | a0001c0002t0024g0182a0001c0002t0025g0183a0001c0002t0037g0259 | 3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.388-3802C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56983999 | ||||||
chr8:56984076
|
T | C | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-3879A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984076 | ||||||
chr8:56984123
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02559.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.388-3926C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984123 | ||||||
chr8:56984805
|
TATC | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.388-4611_388-4609d others(5): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984805 | ||||||
chr8:56984834
|
T | A | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-4637A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984834 | ||||||
chr8:56984861
|
C | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0011g0026others(1): Show | 5 | HG00323.hp2 HG01081.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-4664G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984861 | ||||||
chr8:56984979
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.388-4782G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56984979 | ||||||
chr8:56985100
|
A | G | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-4903T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985100 | ||||||
chr8:56985133
|
T | C | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-4936A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985133 | ||||||
chr8:56985153
|
G | A | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-4956C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985153 | ||||||
chr8:56985200
|
C | A | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-5003G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985200 | ||||||
chr8:56985316
|
T | C | 2 | a0001c0001t0027g0044a0001c0001t0033g0045 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.388-5119A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985316 | ||||||
chr8:56985385
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388-5188A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985385 | ||||||
chr8:56985454
|
C | CACCCTGG others(3): Show |
1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5258_388-5257i others(12): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985454 | ||||||
chr8:56985607
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5410A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985607 | ||||||
chr8:56985679
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5482A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985679 | ||||||
chr8:56985796
|
G | A | 100 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0013others(97): Show | 142 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.388-5599C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985796 | ||||||
chr8:56985818
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.388-5621A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985818 | ||||||
chr8:56985835
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5638C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985835 | ||||||
chr8:56985918
|
C | A | 3 | a0001c0001t0006g0174a0001c0001t0006g0185a0001c0001t0006g0186 | 3 | HG00741.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.388-5721G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985918 | ||||||
chr8:56985941
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-5744G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56985941 | ||||||
chr8:56986018
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.388-5821G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986018 | ||||||
chr8:56986069
|
T | C | 1 | a0001c0001t0009g0018 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-5872A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986069 | ||||||
chr8:56986081
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.388-5884C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986081 | ||||||
chr8:56986361
|
G | A | 48 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(45): Show | 62 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.388-6164C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986361 | ||||||
chr8:56986379
|
A | C | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.388-6182T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986379 | ||||||
chr8:56986408
|
T | C | 1 | a0001c0002t0025g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.388-6211A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986408 | ||||||
chr8:56986411
|
G | T | 1 | a0001c0001t0004g0054 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.388-6214C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986411 | ||||||
chr8:56986579
|
C | A | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-6382G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986579 | ||||||
chr8:56986682
|
A | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0077others(13): Show | 18 | HG01069.hp2 HG01167.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.388-6485T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986682 | ||||||
chr8:56986739
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6460A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986739 | ||||||
chr8:56986740
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6459T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986740 | ||||||
chr8:56986742
|
T | C | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+6457A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986742 | ||||||
chr8:56986769
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.387+6430T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986769 | ||||||
chr8:56986809
|
T | G | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6390A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986809 | ||||||
chr8:56986810
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6389C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986810 | ||||||
chr8:56986846
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6353C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986846 | ||||||
chr8:56986847
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6352G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986847 | ||||||
chr8:56986982
|
T | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.387+6217A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56986982 | ||||||
chr8:56987052
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6147C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987052 | ||||||
chr8:56987054
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6145T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987054 | ||||||
chr8:56987056
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+6143C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987056 | ||||||
chr8:56987262
|
T | C | 2 | a0001c0001t0016g0190a0001c0001t0016g0198 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.387+5937A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987262 | ||||||
chr8:56987311
|
T | G | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+5888A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987311 | ||||||
chr8:56987406
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5793T>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987406 | ||||||
chr8:56987566
|
C | T | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+5633G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987566 | ||||||
chr8:56987616
|
C | A | 85 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(82): Show | 124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.387+5583G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987616 | ||||||
chr8:56987674
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.387+5525A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987674 | ||||||
chr8:56987731
|
C | CT | 54 | a0001c0001t0001g0047a0001c0001t0001g0094a0001c0001t0001g0095others(51): Show | 68 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.387+5467dupA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987731 | ||||||
chr8:56987731
|
CT | C | 39 | a0001c0001t0001g0036a0001c0001t0003g0001a0001c0001t0003g0006others(36): Show | 65 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.387+5467delA | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987731 | ||||||
chr8:56987733
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5466A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987733 | ||||||
chr8:56987736
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.387+5463A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987736 | ||||||
chr8:56987797
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5402G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987797 | ||||||
chr8:56987798
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.387+5401C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987798 | ||||||
chr8:56987803
|
A | C | 36 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.387+5396T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987803 | ||||||
chr8:56987885
|
C | T | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+5314G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987885 | ||||||
chr8:56987994
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.387+5205G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56987994 | ||||||
chr8:56988069
|
C | T | 2 | a0001c0001t0016g0190a0001c0001t0016g0198 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.387+5130G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988069 | ||||||
chr8:56988132
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.387+5067A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988132 | ||||||
chr8:56988134
|
G | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(81): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.387+5065C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988134 | ||||||
chr8:56988414
|
T | C | 2 | a0001c0001t0002g0208a0001c0001t0002g0213 | 2 | HG00423.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.387+4785A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988414 | ||||||
chr8:56988541
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.387+4658A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988541 | ||||||
chr8:56988619
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.387+4580A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988619 | ||||||
chr8:56988684
|
G | A | 1 | a0001c0001t0028g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.387+4515C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988684 | ||||||
chr8:56988697
|
AGATGTTT others(30): Show |
A | 1 | a0001c0001t0004g0049 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.387+4465_387+4501d others(39): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988697 | ||||||
chr8:56988868
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0004g0022 | 4 | NA18967.hp1 NA18975.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+4331A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988868 | ||||||
chr8:56988910
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(220): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.387+4289G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988910 | ||||||
chr8:56988944
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.387+4255G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56988944 | ||||||
chr8:56989200
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0167a0001c0001t0001g0177 | 4 | HG01109.hp2 HG02055.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+3999G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989200 | ||||||
chr8:56989209
|
TAA | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+3988_387+3989d others(4): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989209 | ||||||
chr8:56989350
|
C | T | 5 | a0001c0001t0006g0174a0001c0001t0006g0181a0001c0001t0006g0184others(2): Show | 5 | HG00741.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+3849G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989350 | ||||||
chr8:56989358
|
C | T | 1 | a0001c0001t0030g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.387+3841G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989358 | ||||||
chr8:56989372
|
T | TA | 7 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG00423.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+3826dupT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989372 | ||||||
chr8:56989372
|
TA | T | 100 | a0001c0001t0001g0047a0001c0001t0002g0003a0001c0001t0002g0013others(97): Show | 142 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.387+3826delT | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989372 | ||||||
chr8:56989443
|
T | C | 1 | a0001c0001t0001g0037 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.387+3756A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989443 | ||||||
chr8:56989454
|
G | A | 1 | a0001c0001t0002g0230 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.387+3745C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989454 | ||||||
chr8:56989767
|
A | C | 1 | a0001c0001t0006g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387+3432T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989767 | ||||||
chr8:56989829
|
A | G | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+3370T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989829 | ||||||
chr8:56989872
|
A | G | 11 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233others(8): Show | 11 | HG01123.hp1 NA18941.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.387+3327T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989872 | ||||||
chr8:56989938
|
G | T | 1 | a0001c0002t0024g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387+3261C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56989938 | ||||||
chr8:56990050
|
T | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(34): Show | 62 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.387+3149A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990050 | ||||||
chr8:56990050
|
T | C | 1 | a0001c0001t0008g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.387+3149A>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990050 | ||||||
chr8:56990397
|
T | A | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.387+2802A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990397 | ||||||
chr8:56990425
|
G | A | 1 | a0001c0001t0014g0038 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.387+2774C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990425 | ||||||
chr8:56990534
|
A | C | 36 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 61 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.387+2665T>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990534 | ||||||
chr8:56990639
|
G | T | 1 | a0001c0001t0019g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+2560C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990639 | ||||||
chr8:56990650
|
C | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | NA18956.hp1 NA18983.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.387+2549G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990650 | ||||||
chr8:56990798
|
C | A | 6 | a0001c0001t0006g0174a0001c0001t0006g0181a0001c0001t0006g0184others(3): Show | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+2401G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990798 | ||||||
chr8:56990870
|
A | G | 1 | a0001c0001t0003g0247 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.387+2329T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56990870 | ||||||
chr8:56991075
|
A | G | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2124T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991075 | ||||||
chr8:56991326
|
G | T | 3 | a0001c0001t0027g0044a0001c0001t0028g0046a0001c0001t0033g0045 | 3 | HG02109.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.387+1873C>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991326 | ||||||
chr8:56991329
|
T | TTCAA | 3 | a0001c0001t0001g0086a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01109.hp1 HG01978.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.387+1866_387+1869d others(6): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991329 | ||||||
chr8:56991618
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.387+1581G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56991618 | ||||||
chr8:56992013
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+1186C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992013 | ||||||
chr8:56992042
|
G | C | 1 | a0001c0001t0004g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.387+1157C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992042 | ||||||
chr8:56992142
|
A | G | 5 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1057T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992142 | ||||||
chr8:56992241
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+958G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992241 | ||||||
chr8:56992257
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.387+942C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992257 | ||||||
chr8:56992281
|
C | A | 47 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(44): Show | 61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.387+918G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992281 | ||||||
chr8:56992404
|
T | G | 23 | a0001c0001t0002g0014a0001c0001t0002g0039a0001c0001t0002g0194others(20): Show | 26 | HG00673.hp1 HG01074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.387+795A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992404 | ||||||
chr8:56992452
|
A | AATCCAAA others(30): Show |
1 | a0001c0001t0004g0049 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.387+710_387+746dup others(37): Show |
BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992452 | ||||||
chr8:56992640
|
T | G | 38 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(35): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.387+559A>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992640 | ||||||
chr8:56992641
|
T | A | 38 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(35): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.387+558A>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992641 | ||||||
chr8:56992688
|
A | AC | 27 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0079others(24): Show | 29 | HG00423.hp2 HG01099.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.387+510dupG | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992688 | ||||||
chr8:56992714
|
G | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(220): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.387+485C>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992714 | ||||||
chr8:56992724
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+475T>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992724 | ||||||
chr8:56992738
|
C | T | 47 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(44): Show | 61 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.387+461G>A | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992738 | ||||||
chr8:56992791
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.387+408C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992791 | ||||||
chr8:56992813
|
C | A | 13 | a0001c0001t0006g0181a0001c0001t0006g0184a0001c0001t0006g0185others(10): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+386G>T | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992813 | ||||||
chr8:56992941
|
C | G | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0027g0044others(2): Show | 7 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+258G>C | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992941 | ||||||
chr8:56992986
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.387+213C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56992986 | ||||||
chr8:56993138
|
G | C | 25 | a0001c0001t0003g0001a0001c0001t0003g0006a0001c0001t0003g0009others(22): Show | 50 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.387+61C>G | BPNT2 | ENSG00000104331.9 | transcript | ENST00000262644.9 | protein_coding | 1/4 | chr8 | 56993138 |