geneid | 669 |
---|---|
ensemblid | ENSG00000172331.12 |
hgncid | 1093 |
symbol | BPGM |
name | bisphosphoglycerate mutase |
refseq_nuc | NM_001724.5 |
refseq_prot | NP_001715.1 |
ensembl_nuc | ENST00000344924.8 |
ensembl_prot | ENSP00000342032.3 |
mane_status | MANE Select |
chr | chr7 |
start | 134646853 |
end | 134679816 |
strand | + |
ver | v1.2 |
region | chr7:134646853-134679816 |
region5000 | chr7:134641853-134684816 |
regionname0 | BPGM_chr7_134646853_134679816 |
regionname5000 | BPGM_chr7_134641853_134684816 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 259 | 359 | 81 | 68 | 155 | 16 | 37 | 125 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0002 | 0/0 | 259 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0003 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0004 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 780 | 357 | 81 | 68 | 153 | 16 | 37 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
c0002 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
c0003 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
c0004 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
c0005 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
c0006 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 932 | 329 | 66 | 65 | 152 | 16 | 28 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0002 | 0/0 | 935 | 11 | 5 | 2 | 0 | 0 | 4 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0003 | 0/0 | 935 | 4 | 2 | 0 | 1 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0004 | 0/0 | 932 | 4 | 4 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0005 | 0/0 | 932 | 3 | 0 | 0 | 0 | 0 | 3 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0006 | 0/0 | 929 | 3 | 2 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0007 | 0/0 | 932 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0008 | 0/0 | 950 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0009 | 0/0 | 932 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0010 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0011 | 0/0 | 932 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0012 | 0/0 | 932 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
t0013 | 0/0 | 932 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 49 | 1 | 7 | 30 | 1 | 9 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0002 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0003 | 0/0 | 12 | 0 | 4 | 6 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0004 | 0/0 | 7 | 1 | 3 | 0 | 2 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0005 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0006 | 0/0 | 6 | 3 | 0 | 0 | 0 | 3 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0007 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0011 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0012 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0013 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0015 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0017 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0018 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 780 | 357 | 81 | 68 | 153 | 16 | 37 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0002 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0005 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0002c0003 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0003c0004 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0004c0006 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1711 | 325 | 65 | 65 | 150 | 16 | 27 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0002 | 0/0 | 1714 | 11 | 5 | 2 | 0 | 0 | 4 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0003 | 0/0 | 1714 | 4 | 2 | 0 | 1 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0004 | 0/0 | 1711 | 4 | 4 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0005 | 0/0 | 1711 | 3 | 0 | 0 | 0 | 0 | 3 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0006 | 0/0 | 1708 | 3 | 2 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0007 | 0/0 | 1711 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0008 | 0/0 | 1729 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0009 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0010 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0011 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0001t0012 | 0/0 | 1711 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0002t0001 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0001c0005t0001 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0002c0003t0001 | 0/0 | 1711 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0003c0004t0013 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
a0004c0006t0001 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | copy fasta | chr7 | 134641853 | 134684816 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 45 | 1 | 7 | 28 | 1 | 7 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0002 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0003 | 0/0 | 12 | 0 | 4 | 6 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0004 | 0/0 | 7 | 1 | 3 | 0 | 2 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0005 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0011 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0012 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0015 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0006 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0009g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0001t0012g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0001c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0003c0004t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
a0004c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0125 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03239 | hp1 | a0002 | c0003 | t0001 | g0153 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0148 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0041 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0126 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18960 | hp1 | a0003 | c0004 | t0013 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19009 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19009 | hp2 | a0001 | c0001 | t0009 | g0047 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0145 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19043 | hp2 | a0004 | c0006 | t0001 | g0054 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19070 | hp2 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0105 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0160 | REF | REF | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:134661925
|
C | T | 1 | a0004 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.418C>T | p.Arg140Trp | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/3 | 564/1711 | 418/780 | 140/259 | chr7 | 134661925 | ||
chr7:134678885
|
C | G | 1 | a0003 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.634C>G | p.Leu212Val | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 780/1711 | 634/780 | 212/259 | chr7 | 134678885 | ||
chr7:134678930
|
C | T | 1 | a0002 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.679C>T | p.Arg227Cys | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 825/1711 | 679/780 | 227/259 | chr7 | 134678930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:134661942
|
C | T | 1 | a0001c0005 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.435C>T | p.Cys145Cys | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/3 | 581/1711 | 435/780 | 145/259 | chr7 | 134661942 | ||
chr7:134678971
|
G | A | 1 | a0001c0002 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.720G>A | p.Ala240Ala | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 866/1711 | 720/780 | 240/259 | chr7 | 134678971 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:134646875
|
C | G | 1 | a0003c0004t0013 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14633 | chr7 | 134646875 | |||||
chr7:134646885
|
G | T | 1 | a0001c0001t0007 | 2 | HG03490.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-114G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14623 | chr7 | 134646885 | |||||
chr7:134646886
|
C | T | 1 | a0001c0001t0012 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14622 | chr7 | 134646886 | |||||
chr7:134646897
|
G | GGCT | 2 | a0001c0001t0002a0001c0001t0003 | 15 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-79_-77dupCTG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14585 | INFO_REALIGN_3_PRIME | chr7 | 134646897 | ||||
chr7:134646897
|
G | GGCTGCTG others(11): Show |
1 | a0001c0001t0008 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94_-77dupCTGCTGCT others(10): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14585 | INFO_REALIGN_3_PRIME | chr7 | 134646897 | ||||
chr7:134646897
|
GGCT | G | 1 | a0001c0001t0006 | 3 | HG02970.hp1 HG03195.hp2 NA19070.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79_-77delCTG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14586 | INFO_REALIGN_3_PRIME | chr7 | 134646897 | ||||
chr7:134679118
|
G | A | 2 | a0001c0001t0002a0001c0001t0004 | 15 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*87G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 87 | chr7 | 134679118 | |||||
chr7:134679406
|
C | T | 2 | a0001c0001t0011a0001c0001t0012 | 2 | HG00639.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*375C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 375 | chr7 | 134679406 | |||||
chr7:134679463
|
G | A | 1 | a0001c0001t0009 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 432 | chr7 | 134679463 | |||||
chr7:134679569
|
C | A | 2 | a0001c0001t0005a0001c0001t0010 | 4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*538C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 538 | chr7 | 134679569 | |||||
chr7:134679662
|
T | C | 1 | a0001c0001t0010 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 631 | chr7 | 134679662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:134646971
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-62+34G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134646971 | ||||||
chr7:134647085
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-62+148C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647085 | ||||||
chr7:134647342
|
A | G | 1 | a0001c0001t0001g0049 | 2 | HG00544.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-62+405A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647342 | ||||||
chr7:134647355
|
TATCA | T | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+419_-62+422del others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647355 | ||||||
chr7:134647408
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-62+471G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647408 | ||||||
chr7:134647423
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+486G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647423 | ||||||
chr7:134647835
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+898C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647835 | ||||||
chr7:134647888
|
A | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-62+951A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647888 | ||||||
chr7:134647891
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-62+954G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647891 | ||||||
chr7:134648003
|
G | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0149others(1): Show | 6 | HG01071.hp1 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+1066G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648003 | ||||||
chr7:134648069
|
A | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+1132A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648069 | ||||||
chr7:134648070
|
T | TCC | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+1133_-62+1134i others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648070 | ||||||
chr7:134648071
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+1134T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648071 | ||||||
chr7:134648073
|
C | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+1136C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648073 | ||||||
chr7:134648117
|
C | CT | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1183dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134648117 | |||||
chr7:134648121
|
C | G | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1184C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648121 | ||||||
chr7:134648130
|
TGG | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1194_-62+1195d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648130 | ||||||
chr7:134648131
|
G | GC | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(3): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | ||||||
chr7:134648131
|
G | GTTT | 23 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0037others(20): Show | 47 | HG00597.hp1 HG01099.hp1 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(5): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | ||||||
chr7:134648131
|
G | GTTTT | 3 | a0001c0001t0001g0127a0001c0001t0011g0126a0001c0001t0012g0125 | 3 | HG00639.hp1 NA18522.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | ||||||
chr7:134648131
|
G | GTTTTT | 19 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 24 | HG00280.hp1 HG00642.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(7): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | ||||||
chr7:134648131
|
G | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 6 | NA18960.hp2 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+1194G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | ||||||
chr7:134648132
|
G | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(142): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-62+1195G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648132 | ||||||
chr7:134648137
|
T | G | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1200T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648137 | ||||||
chr7:134648143
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-62+1206G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648143 | ||||||
chr7:134648148
|
G | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+1211G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648148 | ||||||
chr7:134648153
|
C | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+1216C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648153 | ||||||
chr7:134648166
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-62+1229G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648166 | ||||||
chr7:134648321
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-62+1384G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648321 | ||||||
chr7:134648427
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 5 | HG02896.hp1 HG02897.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+1490G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648427 | ||||||
chr7:134648438
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-62+1501T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648438 | ||||||
chr7:134648445
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+1508T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648445 | ||||||
chr7:134648687
|
A | AT | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(133): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-62+1760dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134648687 | |||||
chr7:134648687
|
A | ATT | 5 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0050others(2): Show | 10 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+1759_-62+1760d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134648687 | |||||
chr7:134648925
|
T | G | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-62+1988T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648925 | ||||||
chr7:134649134
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-62+2197A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649134 | ||||||
chr7:134649137
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-62+2200G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649137 | ||||||
chr7:134649171
|
A | AT | 12 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0037others(9): Show | 32 | HG00597.hp1 HG02074.hp2 NA18942.hp2 others(29): Show |
intron_variant | MODIFIER | c.-62+2236dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134649171 | |||||
chr7:134649173
|
TG | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 6 | HG03453.hp2 NA19012.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+2237delG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649173 | ||||||
chr7:134649174
|
G | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-62+2237G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649174 | ||||||
chr7:134649174
|
GT | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 58 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.-62+2248delT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134649174 | |||||
chr7:134649198
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0037others(10): Show | 33 | HG00597.hp1 HG02074.hp2 NA18942.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62+2261C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649198 | ||||||
chr7:134649273
|
T | C | 1 | a0001c0001t0008g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-62+2336T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649273 | ||||||
chr7:134649280
|
T | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-62+2343T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649280 | ||||||
chr7:134649388
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+2451G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649388 | ||||||
chr7:134649489
|
G | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0037others(13): Show | 36 | HG00597.hp1 HG00639.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-62+2552G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649489 | ||||||
chr7:134649534
|
TG | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-62+2599delG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134649534 | |||||
chr7:134649639
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-62+2702A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649639 | ||||||
chr7:134649692
|
A | G | 1 | a0001c0001t0006g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-62+2755A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649692 | ||||||
chr7:134649886
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-62+2949C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649886 | ||||||
chr7:134649905
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+2968C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649905 | ||||||
chr7:134650002
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3065A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650002 | ||||||
chr7:134650010
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3073G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650010 | ||||||
chr7:134650060
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0003g0058 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-62+3123G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650060 | ||||||
chr7:134650088
|
G | T | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+3151G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650088 | ||||||
chr7:134650170
|
C | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3233C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650170 | ||||||
chr7:134650237
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3300C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650237 | ||||||
chr7:134650355
|
G | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-62+3418G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650355 | ||||||
chr7:134650411
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-62+3474G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650411 | ||||||
chr7:134650421
|
G | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-62+3484G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650421 | ||||||
chr7:134650457
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3520A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650457 | ||||||
chr7:134650646
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-62+3709A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650646 | ||||||
chr7:134650786
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3849G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650786 | ||||||
chr7:134650794
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-62+3857G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650794 | ||||||
chr7:134650798
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3861A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650798 | ||||||
chr7:134650805
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-62+3868G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650805 | ||||||
chr7:134650856
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-62+3919C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650856 | ||||||
chr7:134650869
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+3932G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650869 | ||||||
chr7:134650903
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-62+3966C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650903 | ||||||
chr7:134650915
|
A | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-62+3978A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650915 | ||||||
chr7:134650945
|
T | C | 2 | a0001c0001t0006g0062a0001c0001t0006g0063 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-62+4008T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650945 | ||||||
chr7:134650981
|
C | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+4044C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650981 | ||||||
chr7:134651593
|
A | T | 1 | a0001c0001t0011g0126 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-62+4656A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134651593 | ||||||
chr7:134652015
|
T | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0064 | 6 | HG02109.hp2 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+5078T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652015 | ||||||
chr7:134652016
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-62+5079A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652016 | ||||||
chr7:134652045
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-62+5108A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652045 | ||||||
chr7:134652120
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-62+5183C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652120 | ||||||
chr7:134652225
|
G | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0166others(5): Show | 10 | HG00280.hp2 HG01074.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-62+5288G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652225 | ||||||
chr7:134652441
|
C | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+5504C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652441 | ||||||
chr7:134652457
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0099 | 2 | NA18747.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-62+5520A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652457 | ||||||
chr7:134652463
|
T | G | 2 | a0001c0001t0006g0062a0001c0001t0006g0063 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-62+5526T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652463 | ||||||
chr7:134652625
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0001t0001g0066 | 7 | HG01069.hp1 HG01074.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62+5688G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652625 | ||||||
chr7:134652670
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+5733T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652670 | ||||||
chr7:134652706
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-62+5769C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652706 | ||||||
chr7:134652720
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-62+5783C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652720 | ||||||
chr7:134652947
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-62+6010G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652947 | ||||||
chr7:134652960
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+6023A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652960 | ||||||
chr7:134652989
|
C | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+6052C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652989 | ||||||
chr7:134653098
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-62+6161T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134653098 | ||||||
chr7:134653172
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-62+6235T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134653172 | ||||||
chr7:134653201
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0159 | 4 | NA18944.hp2 NA18986.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+6264A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134653201 | ||||||
chr7:134654127
|
T | TAC | 43 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(40): Show | 73 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.-62+7207_-62+7208d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134654127 | |||||
chr7:134654146
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-62+7209G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654146 | ||||||
chr7:134654147
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-62+7210T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654147 | ||||||
chr7:134654149
|
CTGAAGA | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+7219_-62+7224d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134654149 | |||||
chr7:134654150
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7213T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654150 | ||||||
chr7:134654150
|
T | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(81): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+7213T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654150 | ||||||
chr7:134654151
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7214G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654151 | ||||||
chr7:134654151
|
G | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(81): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+7214G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654151 | ||||||
chr7:134654152
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7215A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654152 | ||||||
chr7:134654152
|
AAG | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(81): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+7217_-62+7218d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134654152 | |||||
chr7:134654153
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7216A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654153 | ||||||
chr7:134654154
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7217G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654154 | ||||||
chr7:134654155
|
A | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-62+7218A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654155 | ||||||
chr7:134654319
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-7128A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654319 | ||||||
chr7:134654327
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-7120G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654327 | ||||||
chr7:134654498
|
A | G | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-6949A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654498 | ||||||
chr7:134654688
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-6759G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654688 | ||||||
chr7:134654890
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-61-6557A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654890 | ||||||
chr7:134654988
|
C | G | 1 | a0001c0001t0006g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-61-6459C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654988 | ||||||
chr7:134655238
|
T | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-61-6209T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655238 | ||||||
chr7:134655406
|
A | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-6041A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655406 | ||||||
chr7:134655551
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-5896T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655551 | ||||||
chr7:134655561
|
A | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-61-5886A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655561 | ||||||
chr7:134655581
|
T | A | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-5866T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655581 | ||||||
chr7:134655608
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-5839A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655608 | ||||||
chr7:134655661
|
C | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0039others(15): Show | 27 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-61-5786C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655661 | ||||||
chr7:134655661
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-61-5786C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655661 | ||||||
chr7:134655666
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-61-5781G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655666 | ||||||
chr7:134655738
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-61-5709T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655738 | ||||||
chr7:134655789
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-5658G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655789 | ||||||
chr7:134655928
|
G | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-61-5519G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655928 | ||||||
chr7:134655956
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG02129.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-61-5491G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655956 | ||||||
chr7:134656009
|
G | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-61-5438G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656009 | ||||||
chr7:134656204
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61-5243C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656204 | ||||||
chr7:134656210
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-5237G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656210 | ||||||
chr7:134656486
|
T | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 60 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-61-4961T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656486 | ||||||
chr7:134656602
|
A | G | 1 | a0001c0001t0001g0036 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-61-4845A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656602 | ||||||
chr7:134656615
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-61-4832C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656615 | ||||||
chr7:134656677
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-61-4770T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656677 | ||||||
chr7:134656717
|
C | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-61-4730C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656717 | ||||||
chr7:134656895
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-61-4552G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656895 | ||||||
chr7:134657002
|
G | T | 3 | a0001c0001t0005g0041a0001c0001t0005g0148a0001c0001t0010g0145 | 4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-61-4445G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657002 | ||||||
chr7:134657050
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-61-4397A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657050 | ||||||
chr7:134657058
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0095others(1): Show | 4 | HG00408.hp2 HG00423.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-4389A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657058 | ||||||
chr7:134657317
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-61-4130A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657317 | ||||||
chr7:134657359
|
G | A | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG01099.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-61-4088G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657359 | ||||||
chr7:134657423
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-61-4024T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657423 | ||||||
chr7:134657469
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-61-3978G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657469 | ||||||
chr7:134657524
|
A | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-3923A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657524 | ||||||
chr7:134657775
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-61-3672T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657775 | ||||||
chr7:134657979
|
A | C | 1 | a0001c0001t0001g0057 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-61-3468A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657979 | ||||||
chr7:134657996
|
A | G | 1 | a0001c0001t0001g0046 | 2 | HG00280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-61-3451A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657996 | ||||||
chr7:134658097
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(81): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-61-3350G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658097 | ||||||
chr7:134658174
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0039others(21): Show | 33 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-61-3273T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658174 | ||||||
chr7:134658176
|
G | C | 2 | a0001c0001t0011g0126a0001c0001t0012g0125 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61-3271G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658176 | ||||||
chr7:134658190
|
G | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-3257G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658190 | ||||||
chr7:134658313
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-61-3134G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658313 | ||||||
chr7:134658480
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-61-2967G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658480 | ||||||
chr7:134658573
|
G | T | 1 | a0001c0001t0001g0035 | 2 | NA18992.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-61-2874G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658573 | ||||||
chr7:134658575
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-61-2872G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658575 | ||||||
chr7:134658582
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61-2865G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658582 | ||||||
chr7:134658691
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-61-2756G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658691 | ||||||
chr7:134658701
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-61-2746G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658701 | ||||||
chr7:134658732
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-2715G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658732 | ||||||
chr7:134658739
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-61-2708T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658739 | ||||||
chr7:134658848
|
G | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0002c0003t0001g0153 | 3 | HG01993.hp1 HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-61-2599G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658848 | ||||||
chr7:134658890
|
G | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-2557G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658890 | ||||||
chr7:134658892
|
A | ATTTTTTT others(9): Show |
57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-61-2547_-61-2546i others(18): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(10): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(80): Show | 171 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-61-2547_-61-2546i others(19): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-61-2547_-61-2546i others(18): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-61-2545_-61-2544i others(17): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(9): Show |
22 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 41 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(18): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(10): Show |
7 | a0001c0001t0001g0045a0001c0001t0001g0163a0001c0001t0001g0168others(4): Show | 8 | HG01074.hp2 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(19): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0162a0001c0001t0001g0181others(1): Show | 5 | HG02896.hp1 HG02897.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(20): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(21): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658892
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0189 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-61-2545_-61-2544i others(23): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | |||||
chr7:134658895
|
T | TTTTTTAT others(8): Show |
1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2547_-61-2546i others(17): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658895 | |||||
chr7:134658952
|
G | T | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2495G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658952 | ||||||
chr7:134658977
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-61-2470G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658977 | ||||||
chr7:134659174
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-61-2273G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659174 | ||||||
chr7:134659178
|
C | T | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2269C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659178 | ||||||
chr7:134659235
|
A | G | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2212A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659235 | ||||||
chr7:134659372
|
C | CGT | 11 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0053others(8): Show | 19 | HG02145.hp2 HG02615.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.-61-2036_-61-2035d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
C | CGTGT | 6 | a0001c0001t0001g0021a0001c0001t0001g0050a0001c0001t0001g0072others(3): Show | 8 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61-2038_-61-2035d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
C | CGTGTGT | 4 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0061others(1): Show | 5 | HG00408.hp1 HG00423.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-2040_-61-2035d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
CGT | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(18): Show | 42 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-61-2036_-61-2035d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
CGTGT | C | 34 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 56 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.-61-2038_-61-2035d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
CGTGTGT | C | 10 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0112others(7): Show | 11 | HG01358.hp2 HG02683.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.-61-2040_-61-2035d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
CGTGTGTG others(1): Show |
C | 16 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0038others(13): Show | 36 | HG00597.hp1 HG02074.hp2 HG02615.hp1 others(33): Show |
intron_variant | MODIFIER | c.-61-2042_-61-2035d others(10): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
CGTGTGTG others(11): Show |
C | 9 | a0001c0001t0001g0044a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-61-2052_-61-2035d others(20): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659372
|
CGTGTGTG others(13): Show |
C | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-61-2054_-61-2035d others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | |||||
chr7:134659418
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-61-2029A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659418 | ||||||
chr7:134659430
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-61-2017A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659430 | ||||||
chr7:134659438
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-61-2009G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659438 | ||||||
chr7:134659466
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-61-1981T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659466 | ||||||
chr7:134659475
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0118 | 2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-61-1972A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659475 | ||||||
chr7:134659662
|
C | T | 1 | a0001c0001t0006g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-61-1785C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659662 | ||||||
chr7:134659764
|
C | T | 1 | a0001c0001t0001g0048 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-61-1683C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659764 | ||||||
chr7:134659791
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(52): Show | 90 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-61-1656C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659791 | ||||||
chr7:134659835
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-61-1612T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659835 | ||||||
chr7:134659892
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-61-1555C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659892 | ||||||
chr7:134660004
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-61-1443A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660004 | ||||||
chr7:134660026
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-61-1421G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660026 | ||||||
chr7:134660061
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-61-1386C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660061 | ||||||
chr7:134660138
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-61-1309T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660138 | ||||||
chr7:134660259
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-61-1188A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660259 | ||||||
chr7:134660275
|
T | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-61-1172T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660275 | ||||||
chr7:134660316
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-61-1131T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660316 | ||||||
chr7:134660387
|
A | C | 1 | a0004c0006t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-61-1060A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660387 | ||||||
chr7:134660579
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-61-868C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660579 | ||||||
chr7:134660608
|
G | T | 1 | a0001c0001t0001g0032 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-61-839G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660608 | ||||||
chr7:134660714
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 20 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-61-733G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660714 | ||||||
chr7:134660784
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-61-663C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660784 | ||||||
chr7:134660791
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 52 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.-61-656T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660791 | ||||||
chr7:134660796
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-61-651G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660796 | ||||||
chr7:134661145
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-61-302T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134661145 | ||||||
chr7:134661146
|
AAATTGCC others(12): Show |
A | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-61-299_-61-281del others(19): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134661146 | |||||
chr7:134662256
|
A | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0037others(13): Show | 36 | HG00597.hp1 HG00639.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.601+148A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662256 | ||||||
chr7:134662325
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.601+217C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662325 | ||||||
chr7:134662382
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.601+274C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662382 | ||||||
chr7:134662463
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.601+355T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662463 | ||||||
chr7:134662637
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.601+529A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662637 | ||||||
chr7:134662854
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.601+746A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662854 | ||||||
chr7:134663039
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.601+931G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663039 | ||||||
chr7:134663111
|
C | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601+1003C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663111 | ||||||
chr7:134663140
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.601+1032G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663140 | ||||||
chr7:134663170
|
G | T | 2 | a0001c0001t0011g0126a0001c0001t0012g0125 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+1062G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663170 | ||||||
chr7:134663285
|
C | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601+1177C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663285 | ||||||
chr7:134663368
|
A | ATG | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(79): Show | 170 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.601+1276_601+1277d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134663368 | |||||
chr7:134663368
|
A | ATGTG | 42 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(39): Show | 72 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.601+1274_601+1277d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134663368 | |||||
chr7:134663368
|
A | ATGTGTG | 16 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0112others(13): Show | 22 | HG01358.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.601+1272_601+1277d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134663368 | |||||
chr7:134663524
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.601+1416C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663524 | ||||||
chr7:134663629
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+1521G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663629 | ||||||
chr7:134663654
|
G | T | 1 | a0001c0001t0001g0038 | 2 | NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.601+1546G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663654 | ||||||
chr7:134663663
|
T | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.601+1555T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663663 | ||||||
chr7:134663663
|
T | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.601+1555T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663663 | ||||||
chr7:134663711
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+1603T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663711 | ||||||
chr7:134663724
|
C | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 20 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.601+1616C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663724 | ||||||
chr7:134663762
|
G | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 57 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.601+1654G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663762 | ||||||
chr7:134663923
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+1815C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663923 | ||||||
chr7:134664013
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601+1905A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664013 | ||||||
chr7:134664043
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+1935T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664043 | ||||||
chr7:134664214
|
A | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.601+2106A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664214 | ||||||
chr7:134664303
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+2195G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664303 | ||||||
chr7:134664318
|
C | G | 1 | a0001c0001t0001g0032 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.601+2210C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664318 | ||||||
chr7:134664326
|
C | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.601+2218C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664326 | ||||||
chr7:134664338
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+2230T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664338 | ||||||
chr7:134664437
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601+2329C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664437 | ||||||
chr7:134664468
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0112a0001c0001t0001g0113others(10): Show | 19 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+2360G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664468 | ||||||
chr7:134664548
|
A | AGGTATT | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+2442_601+2443i others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134664548 | |||||
chr7:134664569
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 57 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.601+2461G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664569 | ||||||
chr7:134664611
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.601+2503A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664611 | ||||||
chr7:134664649
|
C | G | 2 | a0001c0001t0011g0126a0001c0001t0012g0125 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+2541C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664649 | ||||||
chr7:134664708
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+2600C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664708 | ||||||
chr7:134664728
|
C | T | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+2620C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664728 | ||||||
chr7:134664790
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.601+2682A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664790 | ||||||
chr7:134664849
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.601+2741A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664849 | ||||||
chr7:134664894
|
C | A | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601+2786C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664894 | ||||||
chr7:134664914
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.601+2806G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664914 | ||||||
chr7:134665016
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0037others(13): Show | 36 | HG00597.hp1 HG00639.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.601+2908T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665016 | ||||||
chr7:134665146
|
G | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0026others(7): Show | 16 | HG01099.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+3038G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665146 | ||||||
chr7:134665172
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+3064G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665172 | ||||||
chr7:134665185
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+3077C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665185 | ||||||
chr7:134665189
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(142): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.601+3081C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665189 | ||||||
chr7:134665247
|
CAAAGTGC others(416): Show |
C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+3148_601+3570d others(2): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665247 | |||||
chr7:134665381
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0168 | 3 | HG01074.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.601+3273G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665381 | ||||||
chr7:134665623
|
T | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0157 | 3 | HG00558.hp2 NA18966.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.601+3515T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665623 | ||||||
chr7:134665645
|
T | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(50): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.601+3537T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665645 | ||||||
chr7:134665649
|
G | GAAAAA | 3 | a0001c0001t0001g0017a0001c0001t0001g0171a0001c0001t0001g0178 | 6 | HG00733.hp2 HG01109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+3561_601+3565d others(7): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | |||||
chr7:134665649
|
G | GAAAAAA | 17 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 31 | HG00280.hp2 HG01074.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.601+3560_601+3565d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | |||||
chr7:134665649
|
G | GAAAAAAA | 7 | a0001c0001t0001g0016a0001c0001t0001g0164a0001c0001t0001g0169others(4): Show | 10 | HG01175.hp2 HG01346.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+3559_601+3565d others(9): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | |||||
chr7:134665649
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.601+3556_601+3565d others(12): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | |||||
chr7:134665811
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.601+3703A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665811 | ||||||
chr7:134665865
|
A | ATTTTCTT others(3): Show |
1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+3777_601+3786d others(12): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665865 | |||||
chr7:134665865
|
ATTTTC | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(92): Show | 151 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.601+3782_601+3786d others(7): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665865 | |||||
chr7:134666022
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+3914T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666022 | ||||||
chr7:134666023
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.601+3915G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666023 | ||||||
chr7:134666081
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.601+3973C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666081 | ||||||
chr7:134666155
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0075 | 4 | HG00140.hp1 HG02698.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4047G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666155 | ||||||
chr7:134666170
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0131 | 5 | HG00323.hp1 HG01081.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+4062G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666170 | ||||||
chr7:134666180
|
A | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02129.hp1 NA18956.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.601+4072A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666180 | ||||||
chr7:134666516
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+4408G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666516 | ||||||
chr7:134666598
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.601+4490G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666598 | ||||||
chr7:134666616
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(58): Show | 90 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.601+4508G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666616 | ||||||
chr7:134666668
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0159 | 4 | NA18944.hp2 NA18986.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4560G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666668 | ||||||
chr7:134666762
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+4654A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666762 | ||||||
chr7:134666802
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.601+4694T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666802 | ||||||
chr7:134666958
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.601+4850T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666958 | ||||||
chr7:134667005
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+4897A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667005 | ||||||
chr7:134667104
|
T | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(58): Show | 90 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.601+4996T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667104 | ||||||
chr7:134667126
|
C | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(83): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.601+5018C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667126 | ||||||
chr7:134667156
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.601+5048T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667156 | ||||||
chr7:134667232
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0039others(21): Show | 33 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.601+5124T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667232 | ||||||
chr7:134667396
|
T | TTATGTGG others(36): Show |
1 | a0001c0001t0001g0139 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+5290_601+5332d others(45): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134667396 | |||||
chr7:134667492
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+5384G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667492 | ||||||
chr7:134667533
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+5425C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667533 | ||||||
chr7:134667567
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601+5459C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667567 | ||||||
chr7:134667677
|
T | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601+5569T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667677 | ||||||
chr7:134667844
|
C | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.601+5736C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667844 | ||||||
chr7:134668068
|
T | TA | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+5961dupA | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134668068 | |||||
chr7:134668350
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+6242T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668350 | ||||||
chr7:134668525
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+6417A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668525 | ||||||
chr7:134668673
|
T | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+6565T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668673 | ||||||
chr7:134668879
|
C | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0162 | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+6771C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668879 | ||||||
chr7:134668891
|
A | AAC | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+6785_601+6786d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134668891 | |||||
chr7:134669059
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+6951G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669059 | ||||||
chr7:134669277
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.601+7169C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669277 | ||||||
chr7:134669321
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601+7213T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669321 | ||||||
chr7:134669506
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+7398G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669506 | ||||||
chr7:134669512
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+7404A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669512 | ||||||
chr7:134669545
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+7437G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669545 | ||||||
chr7:134669776
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+7668A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669776 | ||||||
chr7:134669890
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 57 | HG00597.hp1 HG00639.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.601+7782C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669890 | ||||||
chr7:134670089
|
C | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+7981C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670089 | ||||||
chr7:134670132
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.601+8024T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670132 | ||||||
chr7:134670233
|
G | C | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601+8125G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670233 | ||||||
chr7:134670297
|
G | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+8189G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670297 | ||||||
chr7:134670312
|
G | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0181 | 2 | NA18995.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.601+8204G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670312 | ||||||
chr7:134670396
|
A | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.601+8288A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670396 | ||||||
chr7:134670535
|
A | G | 1 | a0001c0001t0001g0035 | 2 | NA18992.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.602-8318A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670535 | ||||||
chr7:134670627
|
A | AATAG | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.602-8223_602-8220d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134670627 | |||||
chr7:134670657
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.602-8196A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670657 | ||||||
chr7:134670674
|
G | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0039others(25): Show | 37 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.602-8179G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670674 | ||||||
chr7:134670729
|
A | G | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.602-8124A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670729 | ||||||
chr7:134670879
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.602-7974G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670879 | ||||||
chr7:134671105
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.602-7748A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671105 | ||||||
chr7:134671188
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.602-7665T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671188 | ||||||
chr7:134671278
|
G | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0174a0001c0001t0001g0177others(1): Show | 4 | NA18994.hp1 NA18997.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-7575G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671278 | ||||||
chr7:134671285
|
C | T | 1 | a0001c0001t0008g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.602-7568C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671285 | ||||||
chr7:134671363
|
C | CT | 40 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 67 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.602-7474dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134671363 | |||||
chr7:134671363
|
C | CTT | 27 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 53 | HG00597.hp1 HG00639.hp1 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.602-7475_602-7474d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134671363 | |||||
chr7:134671392
|
C | T | 3 | a0001c0001t0005g0041a0001c0001t0005g0148a0001c0001t0010g0145 | 4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-7461C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671392 | ||||||
chr7:134671488
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-7365A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671488 | ||||||
chr7:134671511
|
G | A | 3 | a0001c0001t0005g0041a0001c0001t0005g0148a0001c0001t0010g0145 | 4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-7342G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671511 | ||||||
chr7:134671639
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.602-7214T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671639 | ||||||
chr7:134671890
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.602-6963C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671890 | ||||||
chr7:134672068
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.602-6785T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672068 | ||||||
chr7:134672243
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.602-6610G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672243 | ||||||
chr7:134672257
|
A | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-6596A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672257 | ||||||
chr7:134672276
|
TAACACAG others(13): Show |
T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.602-6561_602-6542d others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134672276 | |||||
chr7:134672414
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-6439T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672414 | ||||||
chr7:134672436
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.602-6417G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672436 | ||||||
chr7:134672437
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.602-6416A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672437 | ||||||
chr7:134672546
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0037others(10): Show | 33 | HG00597.hp1 HG02074.hp2 NA18942.hp2 others(30): Show |
intron_variant | MODIFIER | c.602-6307A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672546 | ||||||
chr7:134672651
|
A | AT | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-6196dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134672651 | |||||
chr7:134672661
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.602-6192A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672661 | ||||||
chr7:134672903
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG01516.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.602-5950G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672903 | ||||||
chr7:134673019
|
A | G | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5834A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673019 | ||||||
chr7:134673025
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.602-5828G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673025 | ||||||
chr7:134673043
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.602-5810G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673043 | ||||||
chr7:134673060
|
A | G | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5793A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673060 | ||||||
chr7:134673123
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.602-5730G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673123 | ||||||
chr7:134673128
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.602-5725C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673128 | ||||||
chr7:134673190
|
T | TAATAAAA others(13): Show |
2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5646_602-5645i others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134673190 | |||||
chr7:134673289
|
T | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5564T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673289 | ||||||
chr7:134673290
|
G | A | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5563G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673290 | ||||||
chr7:134673466
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.602-5387A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673466 | ||||||
chr7:134673532
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.602-5321A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673532 | ||||||
chr7:134673583
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-5270A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673583 | ||||||
chr7:134673903
|
C | CT | 27 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0025others(24): Show | 45 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.602-4928dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134673903 | |||||
chr7:134673903
|
CT | C | 15 | a0001c0001t0001g0031a0001c0001t0001g0084a0001c0001t0001g0091others(12): Show | 15 | HG00099.hp1 HG01099.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.602-4928delT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134673903 | |||||
chr7:134673926
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.602-4927A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673926 | ||||||
chr7:134674165
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(103): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.602-4688A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674165 | ||||||
chr7:134674396
|
C | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4457C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674396 | ||||||
chr7:134674401
|
C | A | 1 | a0001c0001t0008g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.602-4452C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674401 | ||||||
chr7:134674423
|
A | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4430A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674423 | ||||||
chr7:134674428
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0025others(6): Show | 21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-4425T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674428 | ||||||
chr7:134674449
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.602-4404T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674449 | ||||||
chr7:134674451
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.602-4402T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674451 | ||||||
chr7:134674452
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.602-4401G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674452 | ||||||
chr7:134674499
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(28): Show | 52 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.602-4354T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674499 | ||||||
chr7:134674759
|
C | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4094C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674759 | ||||||
chr7:134674844
|
C | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4009C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674844 | ||||||
chr7:134675178
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(117): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.602-3675A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134675178 | ||||||
chr7:134675298
|
T | A | 1 | a0001c0001t0001g0039 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.602-3555T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134675298 | ||||||
chr7:134675466
|
A | G | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-3387A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134675466 | ||||||
chr7:134676433
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.602-2420A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134676433 | ||||||
chr7:134676585
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-2268T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134676585 | ||||||
chr7:134676707
|
C | T | 1 | a0001c0001t0001g0040 | 2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.602-2146C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134676707 | ||||||
chr7:134677122
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.602-1731A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677122 | ||||||
chr7:134677251
|
T | TTTTC | 27 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0039others(24): Show | 36 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.602-1586_602-1583d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134677251 | |||||
chr7:134677532
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.602-1321G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677532 | ||||||
chr7:134677632
|
T | C | 2 | a0001c0001t0005g0041a0001c0001t0005g0148 | 3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-1221T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677632 | ||||||
chr7:134677696
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(87): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.602-1157A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677696 | ||||||
chr7:134677744
|
AAAG | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(28): Show | 52 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.602-1108_602-1106d others(5): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677744 | ||||||
chr7:134677840
|
T | A | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.602-1013T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677840 | ||||||
chr7:134677934
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.602-919T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677934 | ||||||
chr7:134678076
|
C | CTGTT | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0039others(20): Show | 32 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.602-775_602-772dup others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134678076 | |||||
chr7:134678132
|
C | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0025others(6): Show | 21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-721C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678132 | ||||||
chr7:134678218
|
C | T | 2 | a0001c0001t0011g0126a0001c0001t0012g0125 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.602-635C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678218 | ||||||
chr7:134678315
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-538C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678315 | ||||||
chr7:134678330
|
G | A | 1 | a0001c0001t0010g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.602-523G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678330 |