geneid | 28969 |
---|---|
ensemblid | ENSG00000136261.16 |
hgncid | 18808 |
symbol | BZW2 |
name | basic leucine zipper and W2 domains 2 |
refseq_nuc | NM_014038.3 |
refseq_prot | NP_054757.1 |
ensembl_nuc | ENST00000258761.8 |
ensembl_prot | ENSP00000258761.3 |
mane_status | MANE Select |
chr | chr7 |
start | 16646181 |
end | 16706517 |
strand | + |
ver | v1.2 |
region | chr7:16646181-16706517 |
region5000 | chr7:16641181-16711517 |
regionname0 | BZW2_chr7_16646181_16706517 |
regionname5000 | BZW2_chr7_16641181_16711517 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 419 | 418 | 100 | 72 | 180 | 18 | 46 | 136 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1260 | 407 | 91 | 72 | 179 | 18 | 45 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
c0002 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
c0003 | 0/0 | 1260 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
c0004 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
c0005 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
c0006 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
c0007 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 545 | 204 | 23 | 33 | 115 | 8 | 24 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0002 | 0/1 | 545 | 185 | 53 | 35 | 64 | 10 | 22 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0003 | 0/0 | 548 | 11 | 8 | 3 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0004 | 0/0 | 545 | 6 | 6 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0005 | 0/0 | 545 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0006 | 0/0 | 545 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0007 | 0/0 | 545 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0008 | 0/0 | 545 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0009 | 0/0 | 545 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0010 | 0/0 | 545 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
t0011 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0398 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0399 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1260 | 407 | 91 | 72 | 179 | 18 | 45 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0002 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0003 | 0/0 | 1260 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0004 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0005 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0006 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0007 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1804 | 203 | 23 | 33 | 115 | 8 | 23 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0002 | 0/1 | 1804 | 176 | 45 | 35 | 63 | 10 | 22 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0003 | 0/0 | 1807 | 10 | 7 | 3 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0004 | 0/0 | 1804 | 6 | 6 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0005 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0006 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0007 | 0/0 | 1804 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0008 | 0/0 | 1804 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0009 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0010 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0001t0011 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0002t0002 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0002t0003 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0003t0002 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0004t0002 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0005t0001 | 0/0 | 1804 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0006t0002 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
a0001c0007t0002 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | copy fasta | chr7 | 16641181 | 16711517 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0398 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0399 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0006g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0008g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0010g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0011g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0003t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0004t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0006t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0007t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0354 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0399 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0373 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0383 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0396 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0397 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0364 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0371 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0382 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0352 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0317 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0356 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0363 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0376 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0372 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0394 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0379 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0380 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0325 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0355 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02055 | hp1 | a0001 | c0007 | t0002 | g0336 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0388 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0381 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0390 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0313 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0301 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0346 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0389 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0377 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03209 | hp2 | a0001 | c0003 | t0002 | g0295 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0403 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0402 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0357 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0362 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0358 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0385 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0026 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0324 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18906 | hp1 | a0001 | c0002 | t0003 | g0281 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0384 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18943 | hp2 | a0001 | c0001 | t0011 | g0312 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18951 | hp1 | a0001 | c0006 | t0002 | g0054 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0386 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0395 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0391 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0404 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0366 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0392 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0400 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19030 | hp2 | a0001 | c0004 | t0002 | g0298 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0393 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0367 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0387 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0378 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | ASW | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0374 | AFR | ASW | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0351 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | GIH | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | GIH | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0401 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG06807 | hp2 | a0001 | c0003 | t0002 | g0320 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0038 | REF | REF | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0398 | REF | REF | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16674434
|
C | G | 1 | a0001c0007 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.81C>G | p.Pro27Pro | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/12 | 196/1804 | 81/1260 | 27/419 | chr7 | 16674434 | ||
chr7:16689843
|
A | G | 1 | a0001c0006 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.588A>G | p.Ala196Ala | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/12 | 703/1804 | 588/1260 | 196/419 | chr7 | 16689843 | ||
chr7:16694842
|
T | C | 2 | a0001c0003a0001c0004 | 4 | HG02622.hp2 HG03209.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.660T>C | p.Phe220Phe | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/12 | 775/1804 | 660/1260 | 220/419 | chr7 | 16694842 | ||
chr7:16694995
|
G | A | 1 | a0001c0005 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.813G>A | p.Pro271Pro | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/12 | 928/1804 | 813/1260 | 271/419 | chr7 | 16694995 | ||
chr7:16706070
|
G | A | 2 | a0001c0002a0001c0004 | 5 | HG01884.hp2 HG03130.hp2 NA18522.hp2 others(2): Show |
synonymous_variant | LOW | c.1242G>A | p.Ser414Ser | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 1357/1804 | 1242/1260 | 414/419 | chr7 | 16706070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16646182
|
C | G | 1 | a0001c0001t0011 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19262 | chr7 | 16646182 | |||||
chr7:16646202
|
A | ACTG | 2 | a0001c0001t0003a0001c0002t0003 | 11 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-74_-72dupTGC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19219 | INFO_REALIGN_3_PRIME | chr7 | 16646202 | ||||
chr7:16646210
|
T | C | 3 | a0001c0001t0004a0001c0001t0007a0001c0001t0008 | 9 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-86T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19234 | chr7 | 16646210 | |||||
chr7:16646245
|
C | T | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19199 | chr7 | 16646245 | |||||
chr7:16706091
|
G | T | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0008 | 7 | HG01081.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 3 | chr7 | 16706091 | |||||
chr7:16706182
|
C | T | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 94 | chr7 | 16706182 | |||||
chr7:16706311
|
A | G | 1 | a0001c0001t0010 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 223 | chr7 | 16706311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16646335
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8+47G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646335 | ||||||
chr7:16646369
|
G | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 25 | HG01069.hp2 HG01257.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+81G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646369 | ||||||
chr7:16646438
|
C | T | 1 | a0001c0001t0001g0404 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8+150C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646438 | ||||||
chr7:16646502
|
C | A | 1 | a0001c0001t0002g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-8+214C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646502 | ||||||
chr7:16646554
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0037a0001c0001t0002g0038others(49): Show | 53 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8+266G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646554 | ||||||
chr7:16646584
|
C | T | 1 | a0001c0001t0001g0404 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8+296C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646584 | ||||||
chr7:16646635
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | NA18949.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-8+347G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646635 | ||||||
chr7:16646673
|
G | T | 2 | a0001c0001t0002g0403a0001c0001t0010g0402 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-8+385G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646673 | ||||||
chr7:16646847
|
C | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0401 | 3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-8+559C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646847 | ||||||
chr7:16646876
|
T | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-8+588T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646876 | ||||||
chr7:16647041
|
A | C | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8+753A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647041 | ||||||
chr7:16647048
|
C | G | 15 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(12): Show | 15 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8+760C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647048 | ||||||
chr7:16647200
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-8+912G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647200 | ||||||
chr7:16647315
|
G | A | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 304 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.-8+1027G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647315 | ||||||
chr7:16647510
|
G | C | 1 | a0001c0001t0002g0038 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-8+1222G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647510 | ||||||
chr7:16647544
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 305 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.-8+1256A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647544 | ||||||
chr7:16647629
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+1341G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647629 | ||||||
chr7:16647747
|
G | A | 1 | a0001c0001t0007g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+1459G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647747 | ||||||
chr7:16647833
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(10): Show | 14 | HG01069.hp2 HG01257.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+1545A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647833 | ||||||
chr7:16647917
|
C | T | 23 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0068others(20): Show | 23 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8+1629C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647917 | ||||||
chr7:16647917
|
CACTGGGG others(4): Show |
C | 13 | a0001c0001t0001g0005a0001c0001t0002g0001a0001c0001t0002g0010others(10): Show | 19 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+1630_-8+1640del others(11): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647917 | ||||||
chr7:16647929
|
C | G | 13 | a0001c0001t0001g0005a0001c0001t0002g0001a0001c0001t0002g0010others(10): Show | 19 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+1641C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647929 | ||||||
chr7:16647952
|
A | G | 2 | a0001c0001t0002g0388a0001c0001t0002g0389 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-8+1664A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647952 | ||||||
chr7:16648494
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-8+2206A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648494 | ||||||
chr7:16648521
|
C | A | 17 | a0001c0001t0002g0013a0001c0001t0002g0287a0001c0001t0002g0288others(14): Show | 17 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+2233C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648521 | ||||||
chr7:16648601
|
T | G | 1 | a0001c0001t0001g0163 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-8+2313T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648601 | ||||||
chr7:16648641
|
T | G | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8+2353T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648641 | ||||||
chr7:16648685
|
C | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-8+2397C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648685 | ||||||
chr7:16649162
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8+2874G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649162 | ||||||
chr7:16649176
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-8+2888T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649176 | ||||||
chr7:16649204
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-8+2916A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649204 | ||||||
chr7:16649486
|
T | C | 1 | a0001c0001t0001g0404 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8+3198T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649486 | ||||||
chr7:16649578
|
C | T | 1 | a0001c0001t0002g0387 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-8+3290C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649578 | ||||||
chr7:16649962
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-8+3674A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649962 | ||||||
chr7:16649963
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+3675T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649963 | ||||||
chr7:16650002
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8+3714C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650002 | ||||||
chr7:16650032
|
T | G | 10 | a0001c0001t0002g0286a0001c0001t0002g0302a0001c0001t0002g0303others(7): Show | 10 | HG01167.hp1 HG01516.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+3744T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650032 | ||||||
chr7:16650043
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-8+3755T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650043 | ||||||
chr7:16650183
|
T | G | 2 | a0001c0001t0002g0403a0001c0001t0010g0402 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-8+3895T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650183 | ||||||
chr7:16650327
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG00609.hp1 NA18968.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-8+4039G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650327 | ||||||
chr7:16650474
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+4186G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650474 | ||||||
chr7:16650554
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+4266T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650554 | ||||||
chr7:16650591
|
C | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 295 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.-8+4303C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650591 | ||||||
chr7:16650656
|
T | A | 13 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(10): Show | 13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+4368T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650656 | ||||||
chr7:16650732
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-8+4444C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650732 | ||||||
chr7:16650822
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+4534C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650822 | ||||||
chr7:16650907
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-8+4619G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650907 | ||||||
chr7:16650980
|
C | A | 6 | a0001c0001t0001g0273a0001c0001t0003g0270a0001c0001t0003g0271others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+4692C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650980 | ||||||
chr7:16651091
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+4803A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651091 | ||||||
chr7:16651179
|
T | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(56): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+4891T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651179 | ||||||
chr7:16651398
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+5110T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651398 | ||||||
chr7:16651619
|
A | C | 53 | a0001c0001t0001g0148a0001c0001t0002g0003a0001c0001t0002g0037others(50): Show | 54 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8+5331A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651619 | ||||||
chr7:16651696
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+5408G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651696 | ||||||
chr7:16651781
|
C | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-8+5493C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651781 | ||||||
chr7:16651886
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(72): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-8+5598C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651886 | ||||||
chr7:16651887
|
G | A | 13 | a0001c0001t0002g0013a0001c0001t0002g0287a0001c0001t0002g0288others(10): Show | 13 | HG02559.hp2 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+5599G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651887 | ||||||
chr7:16652306
|
G | A | 6 | a0001c0001t0004g0006a0001c0001t0004g0314a0001c0001t0004g0315others(3): Show | 7 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+6018G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652306 | ||||||
chr7:16652359
|
C | CTTGTTCT others(6): Show |
1 | a0001c0001t0002g0009 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8+6076_-8+6088dup others(13): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16652359 | |||||
chr7:16652457
|
T | C | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+6169T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652457 | ||||||
chr7:16652505
|
TTC | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00738.hp2 HG02258.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-8+6221_-8+6222del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16652505 | |||||
chr7:16652538
|
C | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+6250C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652538 | ||||||
chr7:16652539
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG00597.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-8+6251G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652539 | ||||||
chr7:16652631
|
T | A | 1 | a0001c0001t0007g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+6343T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652631 | ||||||
chr7:16652649
|
C | T | 1 | a0001c0001t0002g0386 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-8+6361C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652649 | ||||||
chr7:16652772
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8+6484G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652772 | ||||||
chr7:16652800
|
C | T | 130 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(127): Show | 141 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-8+6512C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652800 | ||||||
chr7:16652986
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+6698C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652986 | ||||||
chr7:16653001
|
A | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(56): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+6713A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653001 | ||||||
chr7:16653034
|
TTG | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(211): Show | 227 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8+6768_-8+6769del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16653034 | |||||
chr7:16653429
|
T | A | 1 | a0001c0001t0002g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+7141T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653429 | ||||||
chr7:16653497
|
G | C | 186 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0035others(183): Show | 198 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.-8+7209G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653497 | ||||||
chr7:16653507
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 304 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.-8+7219A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653507 | ||||||
chr7:16653763
|
T | C | 6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0003g0278others(3): Show | 6 | HG01074.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+7475T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653763 | ||||||
chr7:16653797
|
C | G | 6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0003g0278others(3): Show | 6 | HG01074.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+7509C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653797 | ||||||
chr7:16653891
|
T | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0269 | 3 | HG02165.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+7603T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653891 | ||||||
chr7:16654078
|
C | A | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG02004.hp1 HG02109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+7790C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654078 | ||||||
chr7:16654083
|
CA | C | 77 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.-8+7823delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | |||||
chr7:16654083
|
CAAAA | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0020others(32): Show | 35 | HG01106.hp1 HG01167.hp1 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-8+7820_-8+7823del others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | |||||
chr7:16654083
|
CAAAAA | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(162): Show | 177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.-8+7819_-8+7823del others(5): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | |||||
chr7:16654083
|
CAAAAAA | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0095others(69): Show | 74 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.-8+7818_-8+7823del others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | |||||
chr7:16654341
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+8053T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654341 | ||||||
chr7:16654352
|
T | C | 1 | a0001c0001t0002g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+8064T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654352 | ||||||
chr7:16654435
|
T | C | 1 | a0001c0001t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-8+8147T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654435 | ||||||
chr7:16654473
|
A | G | 56 | a0001c0001t0001g0014a0001c0001t0002g0003a0001c0001t0002g0037others(53): Show | 57 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-8+8185A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654473 | ||||||
chr7:16654509
|
A | AC | 54 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0031others(51): Show | 55 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8+8233dupC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654509 | |||||
chr7:16654509
|
AC | A | 74 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(71): Show | 75 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8+8233delC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654509 | |||||
chr7:16654509
|
ACC | A | 114 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(111): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-8+8232_-8+8233del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654509 | |||||
chr7:16654520
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0404 | 2 | HG02523.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-8+8232C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654520 | ||||||
chr7:16654521
|
C | A | 9 | a0001c0001t0001g0207a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01515.hp2 HG02717.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+8233C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654521 | ||||||
chr7:16654521
|
C | CA | 6 | a0001c0001t0001g0097a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG00609.hp2 HG00735.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+8242dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654521 | |||||
chr7:16654522
|
A | C | 6 | a0001c0001t0001g0205a0001c0001t0001g0264a0001c0001t0003g0278others(3): Show | 6 | HG02896.hp1 HG02897.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+8234A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654522 | ||||||
chr7:16654557
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-8+8269C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654557 | ||||||
chr7:16654594
|
G | A | 1 | a0001c0001t0002g0343 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-8+8306G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654594 | ||||||
chr7:16654680
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-8+8392G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654680 | ||||||
chr7:16654704
|
G | GT | 25 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0147others(22): Show | 25 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8+8430dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654704 | |||||
chr7:16654704
|
GT | G | 117 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-8+8430delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654704 | |||||
chr7:16654745
|
C | G | 1 | a0001c0005t0001g0026 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8+8457C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654745 | ||||||
chr7:16654801
|
A | G | 2 | a0001c0001t0002g0395a0001c0001t0002g0396 | 2 | HG00423.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-8+8513A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654801 | ||||||
chr7:16654864
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(50): Show | 54 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-8+8576G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654864 | ||||||
chr7:16654868
|
A | G | 1 | a0001c0001t0002g0378 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-8+8580A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654868 | ||||||
chr7:16655160
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0208 | 2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-8+8872A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655160 | ||||||
chr7:16655197
|
A | G | 19 | a0001c0001t0001g0014a0001c0001t0001g0273a0001c0001t0001g0276others(16): Show | 19 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+8909A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655197 | ||||||
chr7:16655242
|
A | T | 17 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0273others(14): Show | 17 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+8954A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655242 | ||||||
chr7:16655416
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8+9128A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655416 | ||||||
chr7:16655542
|
C | T | 1 | a0001c0001t0007g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+9254C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655542 | ||||||
chr7:16655594
|
A | G | 13 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(10): Show | 13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+9306A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655594 | ||||||
chr7:16655686
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8+9398C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655686 | ||||||
chr7:16655694
|
C | T | 2 | a0001c0001t0002g0388a0001c0001t0002g0389 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-8+9406C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655694 | ||||||
chr7:16655788
|
G | A | 3 | a0001c0001t0002g0337a0001c0001t0002g0338a0001c0007t0002g0336 | 3 | HG02055.hp1 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-8+9500G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655788 | ||||||
chr7:16655790
|
G | A | 1 | a0001c0001t0007g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+9502G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655790 | ||||||
chr7:16655832
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8+9544T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655832 | ||||||
chr7:16655861
|
G | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(77): Show | 81 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-8+9573G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655861 | ||||||
chr7:16655994
|
CA | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 22 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-9434delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16655994 | |||||
chr7:16656063
|
G | A | 57 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-7-9374G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656063 | ||||||
chr7:16656081
|
A | ATG | 20 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(17): Show | 21 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7-9342_-7-9341dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656081 | |||||
chr7:16656133
|
A | T | 1 | a0001c0001t0001g0255 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-7-9304A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656133 | ||||||
chr7:16656137
|
C | CTATATAT others(7): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-9299_-7-9286dup others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | |||||
chr7:16656137
|
C | CTATATAT others(13): Show |
3 | a0001c0001t0003g0270a0001c0001t0003g0271a0001c0001t0003g0272 | 3 | HG01255.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(20): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | |||||
chr7:16656137
|
C | CTATATAT others(15): Show |
6 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG01074.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(22): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | |||||
chr7:16656137
|
C | CTATATAT others(19): Show |
1 | a0001c0002t0003g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(26): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | |||||
chr7:16656137
|
C | CTATATAT others(21): Show |
2 | a0001c0001t0003g0274a0001c0001t0003g0275 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(28): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | |||||
chr7:16656137
|
C | CTATATAT others(23): Show |
1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(30): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | |||||
chr7:16656143
|
A | G | 14 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(11): Show | 14 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-9294A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656143 | ||||||
chr7:16656150
|
T | TATAC | 57 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656150
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(20): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656150
|
T | TATATATA others(17): Show |
2 | a0001c0001t0007g0091a0001c0001t0009g0110 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(24): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656150
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(26): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656150
|
T | TATATATA others(23): Show |
1 | a0001c0001t0005g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(30): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656150
|
T | TATATATA others(25): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02004.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(32): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656150
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(36): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | |||||
chr7:16656190
|
ATG | A | 13 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(10): Show | 13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-9243_-7-9242del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656190 | |||||
chr7:16656267
|
A | G | 13 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(10): Show | 13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-9170A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656267 | ||||||
chr7:16656317
|
A | C | 1 | a0001c0001t0002g0063 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-7-9120A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656317 | ||||||
chr7:16656506
|
G | A | 2 | a0001c0001t0003g0274a0001c0001t0003g0275 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7-8931G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656506 | ||||||
chr7:16656544
|
A | AGC | 8 | a0001c0001t0002g0008a0001c0001t0002g0033a0001c0001t0002g0034others(5): Show | 9 | HG01109.hp1 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-8882_-7-8881dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656544 | |||||
chr7:16656544
|
AGC | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG02129.hp2 NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-7-8882_-7-8881del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656544 | |||||
chr7:16656548
|
C | T | 1 | a0001c0001t0002g0376 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-7-8889C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656548 | ||||||
chr7:16656551
|
GCGCGCA | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0197a0001c0001t0001g0210 | 3 | HG02004.hp2 HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-7-8884_-7-8879del others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656551 | |||||
chr7:16656552
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-8885C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656552 | ||||||
chr7:16656553
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0211 | 2 | HG01978.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-7-8884G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656553 | ||||||
chr7:16656553
|
GCGCACAC others(7): Show |
G | 9 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0125others(6): Show | 9 | HG00597.hp2 HG00738.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-8882_-7-8869del others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656553 | |||||
chr7:16656553
|
GCGCACAC others(9): Show |
G | 43 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(40): Show | 44 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7-8882_-7-8867del others(16): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656553 | |||||
chr7:16656554
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7-8883C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656554 | ||||||
chr7:16656555
|
G | A | 6 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-8882G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656555 | ||||||
chr7:16656555
|
G | GCA | 20 | a0001c0001t0001g0019a0001c0001t0001g0165a0001c0001t0001g0166others(17): Show | 21 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-8841_-7-8840dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
G | GCACA | 5 | a0001c0001t0002g0289a0001c0001t0002g0343a0001c0001t0002g0371others(2): Show | 5 | HG00741.hp2 HG02056.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8843_-7-8840dup others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
G | GCACACA | 5 | a0001c0001t0002g0013a0001c0001t0002g0291a0001c0001t0002g0297others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-8845_-7-8840dup others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
G | GCACACAC others(1): Show |
6 | a0001c0001t0002g0287a0001c0001t0002g0290a0001c0001t0002g0293others(3): Show | 6 | HG02886.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-8847_-7-8840dup others(8): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0002g0288a0001c0003t0002g0295a0001c0004t0002g0298 | 3 | HG03209.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-8849_-7-8840dup others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
G | GCACACAC others(5): Show |
2 | a0001c0001t0002g0296a0001c0001t0002g0299 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-8851_-7-8840dup others(12): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
GCA | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0020others(163): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-7-8841_-7-8840del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
GCACA | G | 40 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0198others(37): Show | 40 | HG00597.hp1 HG01106.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7-8843_-7-8840del others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
GCACACA | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0259others(5): Show | 9 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-8845_-7-8840del others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656555
|
GCACACAC others(9): Show |
G | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-8855_-7-8840del others(16): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | |||||
chr7:16656557
|
A | G | 13 | a0001c0001t0001g0192a0001c0001t0001g0254a0001c0001t0001g0263others(10): Show | 13 | HG01884.hp2 HG01975.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-8880A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656557 | ||||||
chr7:16656559
|
A | G | 17 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(14): Show | 20 | HG00280.hp2 HG00558.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-8878A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656559 | ||||||
chr7:16656561
|
A | G | 14 | a0001c0001t0001g0175a0001c0001t0001g0197a0001c0001t0001g0203others(11): Show | 15 | HG01081.hp2 HG01891.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-8876A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656561 | ||||||
chr7:16656563
|
A | G | 3 | a0001c0001t0002g0332a0001c0001t0002g0403a0001c0001t0010g0402 | 3 | HG03139.hp2 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-8874A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656563 | ||||||
chr7:16656922
|
A | C | 1 | a0001c0001t0002g0401 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-7-8515A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656922 | ||||||
chr7:16657222
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-7-8215A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657222 | ||||||
chr7:16657223
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-7-8214G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657223 | ||||||
chr7:16657477
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-7-7960A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657477 | ||||||
chr7:16657486
|
C | T | 2 | a0001c0001t0003g0279a0001c0001t0003g0280 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-7-7951C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657486 | ||||||
chr7:16657691
|
T | C | 14 | a0001c0001t0001g0239a0001c0001t0001g0273a0001c0001t0001g0276others(11): Show | 14 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-7746T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657691 | ||||||
chr7:16657710
|
A | G | 376 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(373): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-7-7727A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657710 | ||||||
chr7:16657805
|
A | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0237 | 3 | HG00423.hp2 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-7-7632A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657805 | ||||||
chr7:16657811
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0197a0001c0001t0001g0210 | 3 | HG02004.hp2 HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-7-7626C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657811 | ||||||
chr7:16657813
|
C | A | 69 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(66): Show | 70 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-7-7624C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657813 | ||||||
chr7:16658084
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0002g0319a0001c0001t0009g0110 | 3 | HG02647.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-7353A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658084 | ||||||
chr7:16658196
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-7-7241G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658196 | ||||||
chr7:16658356
|
T | C | 1 | a0001c0001t0003g0271 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-7081T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658356 | ||||||
chr7:16658409
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7-7028C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658409 | ||||||
chr7:16658642
|
C | A | 190 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0035others(187): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-7-6795C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658642 | ||||||
chr7:16658692
|
T | C | 19 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-6745T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658692 | ||||||
chr7:16658883
|
G | GTA | 4 | a0001c0001t0001g0206a0001c0001t0001g0404a0001c0001t0002g0289others(1): Show | 4 | HG02523.hp2 HG02886.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-6538_-7-6537dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16658883 | |||||
chr7:16658883
|
GTA | G | 70 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(67): Show | 71 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7-6538_-7-6537del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16658883 | |||||
chr7:16658934
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-7-6503T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658934 | ||||||
chr7:16659026
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-7-6411C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659026 | ||||||
chr7:16659083
|
G | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-6354G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659083 | ||||||
chr7:16659193
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-7-6244T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659193 | ||||||
chr7:16659223
|
A | T | 3 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0304 | 3 | HG01516.hp2 HG04115.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-7-6214A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659223 | ||||||
chr7:16659288
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7-6149G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659288 | ||||||
chr7:16659838
|
G | T | 1 | a0001c0001t0001g0262 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-7-5599G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659838 | ||||||
chr7:16659852
|
A | AT | 6 | a0001c0001t0001g0014a0001c0001t0001g0273a0001c0001t0002g0149others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-5574dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16659852 | |||||
chr7:16659852
|
AT | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(51): Show | 55 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-7-5574delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16659852 | |||||
chr7:16659857
|
T | A | 15 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0276others(12): Show | 15 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-5580T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659857 | ||||||
chr7:16659858
|
T | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(71): Show | 75 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-7-5579T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659858 | ||||||
chr7:16659888
|
A | C | 16 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0273others(13): Show | 16 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-5549A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659888 | ||||||
chr7:16659958
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0128 | 3 | HG00438.hp1 NA19060.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-7-5479G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659958 | ||||||
chr7:16659972
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-5465G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659972 | ||||||
chr7:16660006
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-7-5431C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660006 | ||||||
chr7:16660008
|
C | T | 12 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0003g0270others(9): Show | 12 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-5429C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660008 | ||||||
chr7:16660010
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-7-5427C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660010 | ||||||
chr7:16660036
|
C | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 300 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-7-5401C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660036 | ||||||
chr7:16660113
|
G | A | 12 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0003g0270others(9): Show | 12 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-5324G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660113 | ||||||
chr7:16660130
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-7-5307G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660130 | ||||||
chr7:16660171
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-7-5266T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660171 | ||||||
chr7:16660229
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-7-5208A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660229 | ||||||
chr7:16660249
|
T | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(67): Show | 71 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7-5188T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660249 | ||||||
chr7:16660260
|
A | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-7-5177A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660260 | ||||||
chr7:16660352
|
A | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0035others(142): Show | 156 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-7-5085A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660352 | ||||||
chr7:16660400
|
T | TA | 128 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(125): Show | 130 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.-7-5020dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16660400 | |||||
chr7:16660400
|
T | TAA | 10 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0028others(7): Show | 11 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-5021_-7-5020dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16660400 | |||||
chr7:16660400
|
TA | T | 8 | a0001c0001t0001g0098a0001c0001t0001g0236a0001c0001t0002g0308others(5): Show | 8 | HG00621.hp1 HG02698.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-5020delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16660400 | |||||
chr7:16660401
|
A | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0249a0001c0001t0007g0301 | 3 | HG02630.hp1 HG04228.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-7-5036A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660401 | ||||||
chr7:16660430
|
C | T | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7-5007C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660430 | ||||||
chr7:16660485
|
T | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 75 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-7-4952T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660485 | ||||||
chr7:16660529
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-4908G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660529 | ||||||
chr7:16660543
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-7-4894G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660543 | ||||||
chr7:16660736
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0002g0319a0001c0001t0009g0110 | 3 | HG02647.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-4701C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660736 | ||||||
chr7:16660741
|
C | G | 9 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-4696C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660741 | ||||||
chr7:16660812
|
A | G | 14 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(11): Show | 14 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-4625A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660812 | ||||||
chr7:16660822
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0035others(77): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-7-4615A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660822 | ||||||
chr7:16660870
|
G | A | 223 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 234 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.-7-4567G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660870 | ||||||
chr7:16660928
|
C | T | 225 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 236 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-7-4509C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660928 | ||||||
chr7:16661023
|
C | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(203): Show | 217 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.-7-4414C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661023 | ||||||
chr7:16661109
|
A | G | 4 | a0001c0001t0002g0009a0001c0001t0002g0363a0001c0001t0002g0374others(1): Show | 5 | HG01243.hp1 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-4328A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661109 | ||||||
chr7:16661131
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-7-4306C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661131 | ||||||
chr7:16661132
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.-7-4305G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661132 | ||||||
chr7:16661173
|
G | A | 205 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(202): Show | 216 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.-7-4264G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661173 | ||||||
chr7:16661260
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0144 | 2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-7-4177C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661260 | ||||||
chr7:16661377
|
A | T | 2 | a0001c0001t0001g0113a0001c0001t0002g0319 | 2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-7-4060A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661377 | ||||||
chr7:16661481
|
G | A | 5 | a0001c0001t0002g0337a0001c0001t0002g0338a0001c0001t0002g0388others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-3956G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661481 | ||||||
chr7:16661520
|
C | A | 2 | a0001c0001t0002g0403a0001c0001t0010g0402 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-3917C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661520 | ||||||
chr7:16661711
|
A | G | 2 | a0001c0001t0002g0335a0001c0003t0002g0320 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-7-3726A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661711 | ||||||
chr7:16661941
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7-3496T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661941 | ||||||
chr7:16661968
|
G | C | 2 | a0001c0001t0002g0403a0001c0001t0010g0402 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-3469G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661968 | ||||||
chr7:16662043
|
T | C | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7-3394T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662043 | ||||||
chr7:16662091
|
T | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(274): Show | 289 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.-7-3346T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662091 | ||||||
chr7:16662179
|
C | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-3258C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662179 | ||||||
chr7:16662364
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-7-3073T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662364 | ||||||
chr7:16662482
|
G | C | 208 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(205): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-7-2955G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662482 | ||||||
chr7:16662496
|
A | G | 1 | a0001c0001t0002g0323 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7-2941A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662496 | ||||||
chr7:16662674
|
C | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(66): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-7-2763C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662674 | ||||||
chr7:16662719
|
T | C | 3 | a0001c0001t0002g0348a0001c0001t0002g0365a0001c0001t0002g0384 | 3 | NA18747.hp2 NA18942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-7-2718T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662719 | ||||||
chr7:16662774
|
A | AAAGG | 4 | a0001c0001t0002g0322a0001c0001t0002g0326a0001c0002t0002g0324others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-2649_-7-2646dup others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16662774 | |||||
chr7:16662814
|
G | A | 2 | a0001c0001t0002g0349a0001c0001t0002g0383 | 2 | HG00323.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-7-2623G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662814 | ||||||
chr7:16662840
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-7-2597G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662840 | ||||||
chr7:16663005
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-2432A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663005 | ||||||
chr7:16663054
|
C | T | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7-2383C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663054 | ||||||
chr7:16663136
|
C | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(200): Show | 214 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-7-2301C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663136 | ||||||
chr7:16663179
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7-2258A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663179 | ||||||
chr7:16663190
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-2247T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663190 | ||||||
chr7:16663231
|
A | G | 1 | a0001c0001t0002g0348 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-7-2206A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663231 | ||||||
chr7:16663242
|
C | T | 78 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(75): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-7-2195C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663242 | ||||||
chr7:16663253
|
CTG | C | 9 | a0001c0001t0001g0095a0001c0001t0002g0068a0001c0001t0002g0073others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-2180_-7-2179del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16663253 | |||||
chr7:16663298
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-7-2139G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663298 | ||||||
chr7:16663327
|
A | G | 2 | a0001c0001t0002g0403a0001c0001t0010g0402 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-2110A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663327 | ||||||
chr7:16663332
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0002g0319a0001c0001t0009g0110 | 3 | HG02647.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-2105A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663332 | ||||||
chr7:16663468
|
C | T | 203 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(200): Show | 214 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-7-1969C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663468 | ||||||
chr7:16663477
|
T | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(201): Show | 215 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.-7-1960T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663477 | ||||||
chr7:16663492
|
C | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(200): Show | 214 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-7-1945C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663492 | ||||||
chr7:16663493
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-7-1944G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663493 | ||||||
chr7:16663604
|
TA | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0283others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-1825delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16663604 | |||||
chr7:16663605
|
A | T | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-7-1832A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663605 | ||||||
chr7:16663700
|
G | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(201): Show | 215 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.-7-1737G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663700 | ||||||
chr7:16663748
|
A | G | 5 | a0001c0001t0004g0006a0001c0001t0004g0314a0001c0001t0004g0315others(2): Show | 6 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1689A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663748 | ||||||
chr7:16663791
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-7-1646C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663791 | ||||||
chr7:16663973
|
G | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0094others(61): Show | 65 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-7-1464G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663973 | ||||||
chr7:16664042
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0072 | 2 | HG02135.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-7-1395A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664042 | ||||||
chr7:16664074
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-1363T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664074 | ||||||
chr7:16664075
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-1362C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664075 | ||||||
chr7:16664076
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-1361T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664076 | ||||||
chr7:16664102
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-7-1335A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664102 | ||||||
chr7:16664127
|
A | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(99): Show | 111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-7-1310A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664127 | ||||||
chr7:16664149
|
GAAA | G | 51 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0101others(48): Show | 51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-7-1286_-7-1284del others(3): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16664149 | |||||
chr7:16664265
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-7-1172C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664265 | ||||||
chr7:16664296
|
A | G | 3 | a0001c0001t0002g0296a0001c0001t0004g0315a0001c0001t0004g0318 | 3 | HG01891.hp1 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-7-1141A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664296 | ||||||
chr7:16664566
|
C | A | 35 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(32): Show | 36 | HG00544.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-7-871C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664566 | ||||||
chr7:16664587
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-7-850A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664587 | ||||||
chr7:16664590
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0059 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-7-847T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664590 | ||||||
chr7:16664594
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0004g0318 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-7-843G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664594 | ||||||
chr7:16664627
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-7-810C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664627 | ||||||
chr7:16664640
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-797T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664640 | ||||||
chr7:16664709
|
A | G | 1 | a0001c0001t0002g0371 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-7-728A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664709 | ||||||
chr7:16664788
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-649A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664788 | ||||||
chr7:16664797
|
C | G | 1 | a0001c0001t0002g0350 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-7-640C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664797 | ||||||
chr7:16664852
|
T | TTATAGTA others(2): Show |
65 | a0001c0001t0001g0014a0001c0001t0001g0113a0001c0001t0001g0154others(62): Show | 65 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.-7-582_-7-574dupTA others(7): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16664852 | |||||
chr7:16664966
|
A | G | 76 | a0001c0001t0001g0014a0001c0001t0001g0113a0001c0001t0001g0154others(73): Show | 76 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-471A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664966 | ||||||
chr7:16665067
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-7-370T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665067 | ||||||
chr7:16665071
|
T | A | 1 | a0001c0001t0002g0395 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-7-366T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665071 | ||||||
chr7:16665071
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-7-366T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665071 | ||||||
chr7:16665290
|
C | T | 2 | a0001c0001t0002g0032a0001c0001t0003g0193 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-7-147C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665290 | ||||||
chr7:16665298
|
T | C | 80 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(77): Show | 81 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(78): Show |
intron_variant | MODIFIER | c.-7-139T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665298 | ||||||
chr7:16665353
|
A | C | 1 | a0001c0001t0002g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-84A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665353 | ||||||
chr7:16665507
|
T | TTG | 17 | a0001c0001t0002g0032a0001c0001t0002g0073a0001c0001t0002g0088others(14): Show | 18 | HG00544.hp2 HG01255.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.58+28_58+29dupGT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | |||||
chr7:16665507
|
T | TTGTG | 11 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0001g0168others(8): Show | 11 | HG01074.hp2 HG01433.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+26_58+29dupGTGT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | |||||
chr7:16665507
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0155a0001c0001t0002g0013a0001c0001t0004g0318 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.58+22_58+29dupGTGT others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | |||||
chr7:16665507
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+20_58+29dupGTGT others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | |||||
chr7:16665638
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0096others(40): Show | 45 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.58+137G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16665638 | ||||||
chr7:16665725
|
A | G | 9 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0001g0161others(6): Show | 9 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+224A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16665725 | ||||||
chr7:16665859
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.58+358A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16665859 | ||||||
chr7:16666128
|
A | T | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0084 | 3 | HG03688.hp2 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.58+627A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666128 | ||||||
chr7:16666159
|
A | G | 5 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0001g0161others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+658A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666159 | ||||||
chr7:16666261
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58+760C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666261 | ||||||
chr7:16666286
|
G | A | 6 | a0001c0001t0002g0290a0001c0001t0002g0300a0001c0001t0002g0319others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+785G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666286 | ||||||
chr7:16666303
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58+802C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666303 | ||||||
chr7:16666310
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+809C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666310 | ||||||
chr7:16666386
|
G | T | 6 | a0001c0001t0002g0290a0001c0001t0002g0300a0001c0001t0002g0319others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+885G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666386 | ||||||
chr7:16666389
|
T | TTTTA | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0122others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+917_58+920dupTT others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | |||||
chr7:16666389
|
T | TTTTATTT others(1): Show |
51 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0120others(48): Show | 52 | HG00140.hp1 HG01081.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.58+913_58+920dupTT others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | |||||
chr7:16666389
|
T | TTTTATTT others(5): Show |
34 | a0001c0001t0001g0027a0001c0001t0001g0113a0001c0001t0001g0119others(31): Show | 34 | HG00597.hp1 HG00738.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+909_58+920dupTT others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | |||||
chr7:16666389
|
T | TTTTATTT others(9): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0029others(56): Show | 60 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.58+905_58+920dupTT others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | |||||
chr7:16666389
|
T | TTTTATTT others(13): Show |
11 | a0001c0001t0001g0024a0001c0001t0001g0179a0001c0001t0001g0194others(8): Show | 11 | HG00621.hp1 HG01884.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+901_58+920dupTT others(18): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | |||||
chr7:16666389
|
TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0181a0001c0001t0002g0340a0001c0001t0002g0349others(5): Show | 8 | HG00323.hp2 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+913_58+920delTT others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | |||||
chr7:16666419
|
T | TTATTTAT others(5): Show |
1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+920_58+921insTT others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666419 | |||||
chr7:16666419
|
T | TTATTTAT others(9): Show |
5 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(2): Show | 5 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+920_58+921insTT others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666419 | |||||
chr7:16666419
|
T | TTATTTAT others(13): Show |
1 | a0001c0001t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58+920_58+921insTT others(18): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666419 | |||||
chr7:16666426
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0002g0032a0001c0001t0003g0193 | 3 | HG02723.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.58+925C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666426 | ||||||
chr7:16666443
|
G | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0273others(17): Show | 20 | HG01106.hp2 HG01516.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+942G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666443 | ||||||
chr7:16666463
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0002g0344a0001c0001t0002g0347others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+962C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666463 | ||||||
chr7:16666505
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(185): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.58+1004C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666505 | ||||||
chr7:16666541
|
T | G | 2 | a0001c0001t0002g0335a0001c0004t0002g0298 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.58+1040T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666541 | ||||||
chr7:16666600
|
A | C | 1 | a0001c0002t0002g0292 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58+1099A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666600 | ||||||
chr7:16666704
|
C | G | 5 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1203C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666704 | ||||||
chr7:16666807
|
T | A | 1 | a0001c0001t0002g0348 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.58+1306T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666807 | ||||||
chr7:16666924
|
T | G | 26 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0162others(23): Show | 27 | HG01106.hp2 HG01243.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.58+1423T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666924 | ||||||
chr7:16667055
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(192): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.58+1554A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667055 | ||||||
chr7:16667071
|
T | A | 1 | a0001c0001t0002g0374 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+1570T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667071 | ||||||
chr7:16667075
|
T | G | 402 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(399): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.58+1574T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667075 | ||||||
chr7:16667132
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0002g0363 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.58+1631A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667132 | ||||||
chr7:16667188
|
A | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(1): Show | 4 | HG03688.hp1 HG03704.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1687A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667188 | ||||||
chr7:16667211
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.58+1710A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667211 | ||||||
chr7:16667230
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0372a0001c0001t0002g0373 | 4 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1729G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667230 | ||||||
chr7:16667239
|
C | A | 26 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0162others(23): Show | 27 | HG01106.hp2 HG01243.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.58+1738C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667239 | ||||||
chr7:16667243
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+1742T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667243 | ||||||
chr7:16667246
|
A | G | 1 | a0001c0001t0002g0305 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58+1745A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667246 | ||||||
chr7:16667279
|
CA | C | 10 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0002g0013others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+1791delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16667279 | |||||
chr7:16667287
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58+1786A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667287 | ||||||
chr7:16667291
|
A | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.58+1790A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667291 | ||||||
chr7:16667292
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+1791A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667292 | ||||||
chr7:16667293
|
C | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0169a0001c0001t0002g0032others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1792C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667293 | ||||||
chr7:16667293
|
C | CA | 7 | a0001c0001t0001g0023a0001c0001t0001g0168a0001c0001t0001g0181others(4): Show | 7 | HG02622.hp2 HG02738.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1803dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16667293 | |||||
chr7:16667304
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.58+1803A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667304 | ||||||
chr7:16667719
|
T | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0064 | 2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.58+2218T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667719 | ||||||
chr7:16667784
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58+2283T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667784 | ||||||
chr7:16667803
|
C | T | 8 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+2302C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667803 | ||||||
chr7:16667833
|
T | G | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.58+2332T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667833 | ||||||
chr7:16667879
|
C | T | 1 | a0001c0001t0010g0402 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.58+2378C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667879 | ||||||
chr7:16667894
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0025 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.58+2393C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667894 | ||||||
chr7:16668007
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2506G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668007 | ||||||
chr7:16668031
|
C | G | 3 | a0001c0001t0002g0341a0001c0001t0002g0360a0001c0001t0002g0394 | 3 | HG01361.hp2 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.58+2530C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668031 | ||||||
chr7:16668122
|
T | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.58+2621T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668122 | ||||||
chr7:16668188
|
G | T | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+2687G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668188 | ||||||
chr7:16668236
|
A | G | 43 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0154others(40): Show | 44 | HG01081.hp2 HG01109.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.58+2735A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668236 | ||||||
chr7:16668403
|
G | T | 75 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0027others(72): Show | 77 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.58+2902G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668403 | ||||||
chr7:16668437
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58+2936T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668437 | ||||||
chr7:16668528
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.58+3027T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668528 | ||||||
chr7:16668687
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0002g0344a0001c0001t0002g0347others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3186C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668687 | ||||||
chr7:16668795
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.58+3294C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668795 | ||||||
chr7:16668813
|
T | C | 1 | a0001c0001t0002g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.58+3312T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668813 | ||||||
chr7:16668838
|
C | G | 1 | a0001c0001t0002g0329 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.58+3337C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668838 | ||||||
chr7:16668983
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.58+3482A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668983 | ||||||
chr7:16669043
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+3542G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669043 | ||||||
chr7:16669075
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.58+3574G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669075 | ||||||
chr7:16669079
|
G | T | 5 | a0001c0001t0001g0095a0001c0001t0002g0068a0001c0001t0002g0073others(2): Show | 5 | HG00544.hp2 NA18945.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+3578G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669079 | ||||||
chr7:16669084
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.58+3583T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669084 | ||||||
chr7:16669114
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0113a0001c0001t0001g0155others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3613T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669114 | ||||||
chr7:16669137
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0002g0039a0001c0001t0002g0339others(5): Show | 9 | HG02132.hp2 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3636T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669137 | ||||||
chr7:16669186
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.58+3685C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669186 | ||||||
chr7:16669194
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58+3693C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669194 | ||||||
chr7:16669286
|
C | G | 1 | a0001c0001t0002g0387 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.58+3785C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669286 | ||||||
chr7:16669341
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0059 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.58+3840C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669341 | ||||||
chr7:16669364
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.58+3863G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669364 | ||||||
chr7:16669492
|
A | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+3991A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669492 | ||||||
chr7:16669520
|
A | G | 4 | a0001c0001t0001g0018a0001c0001t0002g0344a0001c0001t0002g0347others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4019A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669520 | ||||||
chr7:16669621
|
TC | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.58+4122delC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16669621 | |||||
chr7:16669649
|
A | G | 10 | a0001c0001t0002g0080a0001c0001t0002g0302a0001c0001t0002g0303others(7): Show | 10 | HG01106.hp2 HG01516.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+4148A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669649 | ||||||
chr7:16669819
|
A | G | 1 | a0001c0001t0010g0402 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.58+4318A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669819 | ||||||
chr7:16670083
|
T | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(185): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.59-4329T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670083 | ||||||
chr7:16670099
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.59-4313G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670099 | ||||||
chr7:16670104
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-4308G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670104 | ||||||
chr7:16670154
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.59-4258A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670154 | ||||||
chr7:16670175
|
G | T | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.59-4237G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670175 | ||||||
chr7:16670430
|
T | C | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3982T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670430 | ||||||
chr7:16670482
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0002g0032a0001c0001t0003g0193 | 3 | HG02723.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.59-3930T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670482 | ||||||
chr7:16670528
|
A | G | 34 | a0001c0001t0001g0027a0001c0001t0001g0216a0001c0001t0001g0283others(31): Show | 35 | HG01081.hp2 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.59-3884A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670528 | ||||||
chr7:16670677
|
T | G | 1 | a0001c0004t0002g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-3735T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670677 | ||||||
chr7:16670678
|
A | T | 1 | a0001c0004t0002g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-3734A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670678 | ||||||
chr7:16670797
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(1): Show | 4 | HG03688.hp1 HG03704.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3615G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670797 | ||||||
chr7:16670908
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.59-3504C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670908 | ||||||
chr7:16670940
|
C | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0064 | 2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.59-3472C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670940 | ||||||
chr7:16670941
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(100): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.59-3471A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670941 | ||||||
chr7:16671254
|
A | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3158A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671254 | ||||||
chr7:16671295
|
C | G | 5 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0185others(2): Show | 5 | HG00735.hp1 HG01981.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3117C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671295 | ||||||
chr7:16671444
|
C | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0043a0001c0001t0002g0059others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-2968C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671444 | ||||||
chr7:16671445
|
G | A | 6 | a0001c0001t0002g0290a0001c0001t0002g0300a0001c0001t0002g0319others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-2967G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671445 | ||||||
chr7:16671503
|
A | G | 1 | a0001c0001t0004g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.59-2909A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671503 | ||||||
chr7:16671534
|
C | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-2878C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671534 | ||||||
chr7:16671593
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.59-2819G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671593 | ||||||
chr7:16671679
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.59-2733C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671679 | ||||||
chr7:16671813
|
C | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.59-2599C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671813 | ||||||
chr7:16671814
|
C | T | 12 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0001g0168others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2598C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671814 | ||||||
chr7:16671895
|
C | A | 48 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0113others(45): Show | 49 | HG01074.hp2 HG01106.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.59-2517C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671895 | ||||||
chr7:16671930
|
C | CA | 26 | a0001c0001t0001g0023a0001c0001t0001g0094a0001c0001t0001g0099others(23): Show | 27 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.59-2465dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16671930
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0289a0001c0005t0001g0026 | 2 | HG02886.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.59-2474_59-2465dup others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16671930
|
C | CAAAAAAA others(4): Show |
29 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG01106.hp2 HG01516.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-2475_59-2465dup others(11): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16671930
|
C | CAAAAAAA others(5): Show |
98 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0019others(95): Show | 100 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.59-2476_59-2465dup others(12): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16671930
|
C | CAAAAAAA others(6): Show |
42 | a0001c0001t0001g0020a0001c0001t0001g0123a0001c0001t0001g0130others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.59-2477_59-2465dup others(13): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16671930
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0015a0001c0001t0002g0296a0001c0001t0002g0332 | 3 | HG02559.hp2 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.59-2478_59-2465dup others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16671930
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0376a0001c0001t0002g0389 | 2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.59-2479_59-2465dup others(15): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | |||||
chr7:16672208
|
A | G | 47 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0113others(44): Show | 48 | HG01074.hp2 HG01106.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-2204A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672208 | ||||||
chr7:16672237
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0004g0318 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-2175A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672237 | ||||||
chr7:16672268
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0216a0001c0001t0002g0012others(1): Show | 5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2144C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672268 | ||||||
chr7:16672389
|
G | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.59-2023G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672389 | ||||||
chr7:16672586
|
G | T | 1 | a0001c0001t0002g0374 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-1826G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672586 | ||||||
chr7:16672605
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-1807C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672605 | ||||||
chr7:16672708
|
A | G | 6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(3): Show | 6 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1704A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672708 | ||||||
chr7:16672850
|
C | A | 1 | a0001c0004t0002g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-1562C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672850 | ||||||
chr7:16672856
|
ACTTCTGC others(107): Show |
A | 1 | a0001c0004t0002g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-1555_59-1442del | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672856 | ||||||
chr7:16672896
|
A | C | 1 | a0001c0001t0002g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.59-1516A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672896 | ||||||
chr7:16672952
|
C | CT | 31 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0287others(28): Show | 31 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.59-1449dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16672952 | |||||
chr7:16672999
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.59-1413G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672999 | ||||||
chr7:16673076
|
G | A | 9 | a0001c0001t0002g0080a0001c0001t0002g0302a0001c0001t0002g0303others(6): Show | 9 | HG01106.hp2 HG01516.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-1336G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673076 | ||||||
chr7:16673082
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59-1330A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673082 | ||||||
chr7:16673099
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0038 | 3 | HG01070.hp2 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.59-1313A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673099 | ||||||
chr7:16673105
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0161 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.59-1307C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673105 | ||||||
chr7:16673150
|
G | C | 1 | a0001c0001t0002g0397 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.59-1262G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673150 | ||||||
chr7:16673182
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.59-1230G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673182 | ||||||
chr7:16673188
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59-1224C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673188 | ||||||
chr7:16673193
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.59-1219G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673193 | ||||||
chr7:16673202
|
T | C | 6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(3): Show | 6 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1210T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673202 | ||||||
chr7:16673235
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(96): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.59-1177C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673235 | ||||||
chr7:16673236
|
A | G | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.59-1176A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673236 | ||||||
chr7:16673254
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0113a0001c0001t0001g0155others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-1158T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673254 | ||||||
chr7:16673331
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.59-1081T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673331 | ||||||
chr7:16673338
|
A | G | 1 | a0001c0001t0002g0376 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.59-1074A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673338 | ||||||
chr7:16673346
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.59-1066C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673346 | ||||||
chr7:16673619
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.59-793C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673619 | ||||||
chr7:16673674
|
C | A | 1 | a0001c0001t0005g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-738C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673674 | ||||||
chr7:16673687
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.59-725G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673687 | ||||||
chr7:16673721
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.59-691A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673721 | ||||||
chr7:16673961
|
AC | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.59-450delC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673961 | ||||||
chr7:16673963
|
T | C | 11 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0160others(8): Show | 11 | HG02004.hp1 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-449T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673963 | ||||||
chr7:16674132
|
T | C | 45 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 46 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.59-280T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674132 | ||||||
chr7:16674143
|
A | C | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.59-269A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674143 | ||||||
chr7:16674196
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0002g0344a0001c0001t0002g0347others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-216G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674196 | ||||||
chr7:16674203
|
A | G | 1 | a0001c0001t0002g0390 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.59-209A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674203 | ||||||
chr7:16674308
|
A | AT | 194 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(191): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.59-95dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16674308 | |||||
chr7:16674361
|
C | T | 1 | a0001c0001t0011g0312 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.59-51C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674361 | ||||||
chr7:16674672
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.235+84A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674672 | ||||||
chr7:16674775
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0259 | 2 | HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.235+187T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674775 | ||||||
chr7:16674852
|
G | A | 14 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0332others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+264G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674852 | ||||||
chr7:16674967
|
T | A | 13 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0332others(10): Show | 13 | HG01074.hp2 HG01243.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+379T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674967 | ||||||
chr7:16675029
|
AT | A | 23 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0123others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.235+445delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16675029 | |||||
chr7:16675112
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.235+524A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675112 | ||||||
chr7:16675168
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0216a0001c0001t0002g0012others(1): Show | 5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+580T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675168 | ||||||
chr7:16675349
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(138): Show | 144 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.235+761A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675349 | ||||||
chr7:16675352
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+764C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675352 | ||||||
chr7:16675353
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.235+765G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675353 | ||||||
chr7:16675419
|
C | T | 2 | a0001c0001t0002g0365a0001c0001t0002g0384 | 2 | NA18942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.235+831C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675419 | ||||||
chr7:16675491
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.235+903G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675491 | ||||||
chr7:16675579
|
G | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+991G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675579 | ||||||
chr7:16675736
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235+1148C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675736 | ||||||
chr7:16675737
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(125): Show | 131 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.235+1149A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675737 | ||||||
chr7:16675832
|
C | T | 6 | a0001c0001t0001g0156a0001c0001t0002g0033a0001c0001t0002g0034others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+1244C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675832 | ||||||
chr7:16675854
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0256a0001c0001t0001g0258 | 3 | HG01261.hp1 HG01361.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.235+1266C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675854 | ||||||
chr7:16675885
|
G | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0094others(64): Show | 68 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.235+1297G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675885 | ||||||
chr7:16675885
|
G | T | 2 | a0001c0001t0002g0344a0001c0001t0002g0347 | 2 | HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.235+1297G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675885 | ||||||
chr7:16675895
|
C | T | 1 | a0001c0001t0002g0009 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.235+1307C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675895 | ||||||
chr7:16675945
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0006g0152 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.235+1357G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675945 | ||||||
chr7:16675978
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(132): Show | 137 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.235+1390T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675978 | ||||||
chr7:16676035
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.235+1447C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676035 | ||||||
chr7:16676067
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.235+1479C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676067 | ||||||
chr7:16676284
|
C | T | 7 | a0001c0001t0002g0328a0001c0001t0002g0330a0001c0001t0002g0331others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1696C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676284 | ||||||
chr7:16676293
|
A | G | 2 | a0001c0001t0002g0061a0001c0001t0002g0064 | 2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.235+1705A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676293 | ||||||
chr7:16676411
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(125): Show | 131 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.235+1823A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676411 | ||||||
chr7:16676503
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(125): Show | 131 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.235+1915A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676503 | ||||||
chr7:16676520
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235+1932A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676520 | ||||||
chr7:16676527
|
A | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(124): Show | 129 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.235+1939A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676527 | ||||||
chr7:16676580
|
T | C | 10 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(7): Show | 10 | HG01074.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+1992T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676580 | ||||||
chr7:16676586
|
ATG | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(122): Show | 127 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.235+2000_235+2001d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16676586 | |||||
chr7:16676642
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(137): Show | 142 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.235+2054G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676642 | ||||||
chr7:16677051
|
C | CT | 13 | a0001c0001t0001g0104a0001c0001t0001g0126a0001c0001t0001g0161others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+2480dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16677051 | |||||
chr7:16677051
|
C | CTT | 106 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(103): Show | 108 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.235+2479_235+2480d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16677051 | |||||
chr7:16677051
|
CTTTTTTT | C | 6 | a0001c0001t0002g0328a0001c0001t0002g0330a0001c0001t0002g0331others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+2474_235+2480d others(9): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16677051 | |||||
chr7:16677153
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(111): Show | 116 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.235+2565A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677153 | ||||||
chr7:16677219
|
T | C | 13 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+2631T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677219 | ||||||
chr7:16677346
|
C | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2758C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677346 | ||||||
chr7:16677398
|
C | A | 13 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+2810C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677398 | ||||||
chr7:16677444
|
A | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0094others(74): Show | 78 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.235+2856A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677444 | ||||||
chr7:16677450
|
G | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2862G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677450 | ||||||
chr7:16677477
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(100): Show | 104 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.235+2889G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677477 | ||||||
chr7:16677510
|
G | A | 1 | a0001c0001t0010g0402 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.235+2922G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677510 | ||||||
chr7:16677528
|
G | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(122): Show | 127 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.235+2940G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677528 | ||||||
chr7:16677569
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.235+2981G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677569 | ||||||
chr7:16677640
|
C | T | 1 | a0001c0003t0002g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.235+3052C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677640 | ||||||
chr7:16677641
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 122 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.235+3053G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677641 | ||||||
chr7:16677781
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235+3193A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677781 | ||||||
chr7:16677798
|
G | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 122 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.235+3210G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677798 | ||||||
chr7:16677800
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 122 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.235+3212G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677800 | ||||||
chr7:16677821
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0002g0032 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.235+3233A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677821 | ||||||
chr7:16677901
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.235+3313A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677901 | ||||||
chr7:16677918
|
A | G | 8 | a0001c0001t0002g0008a0001c0001t0002g0039a0001c0001t0002g0339others(5): Show | 9 | HG02132.hp2 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+3330A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677918 | ||||||
chr7:16677945
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.236-3356A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677945 | ||||||
chr7:16677988
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(116): Show | 121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3313G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677988 | ||||||
chr7:16678055
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(116): Show | 121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3246C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678055 | ||||||
chr7:16678087
|
C | CT | 26 | a0001c0001t0001g0014a0001c0001t0001g0095a0001c0001t0001g0126others(23): Show | 26 | HG00544.hp2 HG00597.hp2 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-3189dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | |||||
chr7:16678087
|
C | CTT | 87 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(84): Show | 88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.236-3190_236-3189d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | |||||
chr7:16678087
|
C | CTTT | 9 | a0001c0001t0001g0016a0001c0001t0001g0170a0001c0001t0001g0171others(6): Show | 9 | HG00735.hp1 HG02523.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-3191_236-3189d others(5): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | |||||
chr7:16678087
|
CT | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0159others(12): Show | 16 | HG00323.hp1 HG01081.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.236-3189delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | |||||
chr7:16678087
|
CTTTTTT | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-3194_236-3189d others(8): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | |||||
chr7:16678112
|
T | A | 2 | a0001c0001t0002g0344a0001c0001t0002g0347 | 2 | HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.236-3189T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678112 | ||||||
chr7:16678117
|
C | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(115): Show | 120 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.236-3184C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678117 | ||||||
chr7:16678122
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-3179G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678122 | ||||||
chr7:16678155
|
C | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-3146C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678155 | ||||||
chr7:16678165
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(116): Show | 121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3136A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678165 | ||||||
chr7:16678210
|
G | C | 3 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0001t0002g0389 | 3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.236-3091G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678210 | ||||||
chr7:16678241
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(115): Show | 120 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.236-3060G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678241 | ||||||
chr7:16678336
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(116): Show | 121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-2965C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678336 | ||||||
chr7:16678350
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-2951G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678350 | ||||||
chr7:16678360
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(116): Show | 121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-2941T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678360 | ||||||
chr7:16678362
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0132 | 2 | NA18952.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.236-2939G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678362 | ||||||
chr7:16678363
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.236-2938C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678363 | ||||||
chr7:16678598
|
C | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-2703C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678598 | ||||||
chr7:16678652
|
C | T | 1 | a0001c0001t0002g0400 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.236-2649C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678652 | ||||||
chr7:16678765
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0002g0067a0001c0001t0002g0343others(3): Show | 6 | HG02056.hp2 NA18950.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-2536C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678765 | ||||||
chr7:16678795
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(108): Show | 113 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.236-2506G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678795 | ||||||
chr7:16678819
|
C | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-2482C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678819 | ||||||
chr7:16678830
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.236-2471A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678830 | ||||||
chr7:16678840
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0267a0001c0001t0002g0296 | 3 | HG00738.hp2 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.236-2461G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678840 | ||||||
chr7:16678959
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(101): Show | 105 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.236-2342G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678959 | ||||||
chr7:16679025
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-2276G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679025 | ||||||
chr7:16679029
|
G | A | 1 | a0001c0001t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.236-2272G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679029 | ||||||
chr7:16679071
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.236-2230T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679071 | ||||||
chr7:16679201
|
T | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(20): Show | 24 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.236-2100T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679201 | ||||||
chr7:16679211
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.236-2090G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679211 | ||||||
chr7:16679222
|
A | G | 15 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(12): Show | 15 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-2079A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679222 | ||||||
chr7:16679343
|
C | T | 1 | a0001c0001t0002g0328 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.236-1958C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679343 | ||||||
chr7:16679364
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(5): Show | 9 | HG02257.hp1 HG02559.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-1937C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679364 | ||||||
chr7:16679448
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(99): Show | 103 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.236-1853T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679448 | ||||||
chr7:16679492
|
T | C | 1 | a0001c0001t0002g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236-1809T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679492 | ||||||
chr7:16679523
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(130): Show | 136 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.236-1778T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679523 | ||||||
chr7:16679675
|
T | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(102): Show | 106 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.236-1626T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679675 | ||||||
chr7:16679744
|
C | A | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.236-1557C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679744 | ||||||
chr7:16679785
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.236-1516A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679785 | ||||||
chr7:16679855
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0002g0296 | 2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.236-1446G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679855 | ||||||
chr7:16679961
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-1340G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679961 | ||||||
chr7:16680061
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-1240C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680061 | ||||||
chr7:16680101
|
C | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.236-1200C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680101 | ||||||
chr7:16680114
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(115): Show | 119 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.236-1187G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680114 | ||||||
chr7:16680132
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-1169G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680132 | ||||||
chr7:16680139
|
C | A | 1 | a0001c0001t0001g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.236-1162C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680139 | ||||||
chr7:16680159
|
G | A | 14 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-1142G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680159 | ||||||
chr7:16680241
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.236-1060C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680241 | ||||||
chr7:16680292
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(143): Show | 149 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.236-1009T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680292 | ||||||
chr7:16680303
|
T | C | 6 | a0001c0001t0001g0156a0001c0001t0002g0033a0001c0001t0002g0034others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-998T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680303 | ||||||
chr7:16680363
|
T | C | 1 | a0001c0001t0002g0368 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.236-938T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680363 | ||||||
chr7:16680402
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0146 | 2 | NA18963.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.236-899C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680402 | ||||||
chr7:16680450
|
A | G | 1 | a0001c0001t0002g0368 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.236-851A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680450 | ||||||
chr7:16680455
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0002g0296 | 2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.236-846A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680455 | ||||||
chr7:16680501
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.236-800A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680501 | ||||||
chr7:16680591
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.236-710G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680591 | ||||||
chr7:16680648
|
T | C | 5 | a0001c0001t0001g0199a0001c0001t0001g0213a0001c0001t0001g0218others(2): Show | 5 | HG02129.hp1 NA18940.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-653T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680648 | ||||||
chr7:16680719
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-582A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680719 | ||||||
chr7:16680748
|
G | A | 2 | a0001c0001t0002g0307a0001c0001t0002g0308 | 2 | HG01952.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.236-553G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680748 | ||||||
chr7:16680968
|
G | A | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(25): Show | 30 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.236-333G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680968 | ||||||
chr7:16680975
|
A | G | 10 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(7): Show | 10 | HG01074.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-326A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680975 | ||||||
chr7:16681028
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0142 | 2 | NA18940.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.236-273G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16681028 | ||||||
chr7:16681086
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0006g0152 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.236-215G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16681086 | ||||||
chr7:16681227
|
A | T | 1 | a0001c0001t0007g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.236-74A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16681227 | ||||||
chr7:16681674
|
A | C | 1 | a0001c0001t0002g0310 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.339+270A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681674 | ||||||
chr7:16681677
|
C | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+273C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681677 | ||||||
chr7:16681715
|
C | A | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339+311C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681715 | ||||||
chr7:16681757
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(177): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.339+353A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681757 | ||||||
chr7:16681876
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0273others(9): Show | 12 | HG01255.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+472C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681876 | ||||||
chr7:16682104
|
G | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0094others(65): Show | 69 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.340-676G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682104 | ||||||
chr7:16682156
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(101): Show | 105 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.340-624A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682156 | ||||||
chr7:16682172
|
A | G | 6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0334others(3): Show | 6 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-608A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682172 | ||||||
chr7:16682345
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.340-435A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682345 | ||||||
chr7:16682348
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.340-432A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682348 | ||||||
chr7:16682398
|
A | T | 6 | a0001c0001t0001g0156a0001c0001t0002g0033a0001c0001t0002g0034others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-382A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682398 | ||||||
chr7:16682435
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(160): Show | 166 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.340-345G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682435 | ||||||
chr7:16682438
|
G | A | 361 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.340-342G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682438 | ||||||
chr7:16682473
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.340-307G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682473 | ||||||
chr7:16682473
|
G | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340-307G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682473 | ||||||
chr7:16682476
|
A | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0002g0079 | 3 | HG00738.hp2 HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.340-304A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682476 | ||||||
chr7:16682551
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.340-229A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682551 | ||||||
chr7:16682631
|
A | T | 39 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(36): Show | 41 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.340-149A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682631 | ||||||
chr7:16682721
|
A | G | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.340-59A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682721 | ||||||
chr7:16682728
|
A | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(161): Show | 167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.340-52A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682728 | ||||||
chr7:16682745
|
G | A | 41 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(38): Show | 43 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-35G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682745 | ||||||
chr7:16682767
|
G | GT | 44 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(41): Show | 46 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(43): Show |
splice_acceptor_variant&intron_variant | HIGH | c.340-3dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 16682767 | |||||
chr7:16682869
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.405+24A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682869 | ||||||
chr7:16682925
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.405+80C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682925 | ||||||
chr7:16682938
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.405+93C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682938 | ||||||
chr7:16682963
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.405+118C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682963 | ||||||
chr7:16683050
|
C | G | 1 | a0001c0001t0002g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.405+205C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683050 | ||||||
chr7:16683063
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.405+218G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683063 | ||||||
chr7:16683167
|
G | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+322G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683167 | ||||||
chr7:16683175
|
A | G | 41 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(38): Show | 43 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.405+330A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683175 | ||||||
chr7:16683266
|
T | G | 10 | a0001c0001t0001g0283a0001c0001t0002g0323a0001c0001t0002g0326others(7): Show | 10 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.405+421T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683266 | ||||||
chr7:16683333
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405+488A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683333 | ||||||
chr7:16683377
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.405+532A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683377 | ||||||
chr7:16683497
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(258): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.405+652G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683497 | ||||||
chr7:16683503
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(161): Show | 167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.405+658T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683503 | ||||||
chr7:16683542
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.405+697G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683542 | ||||||
chr7:16683580
|
G | A | 3 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0003g0193 | 3 | HG02723.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.405+735G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683580 | ||||||
chr7:16683592
|
A | G | 5 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0084others(2): Show | 5 | HG01981.hp2 HG02300.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.405+747A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683592 | ||||||
chr7:16683688
|
C | T | 2 | a0001c0001t0002g0068a0001c0001t0002g0075 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.405+843C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683688 | ||||||
chr7:16683698
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0273a0001c0001t0002g0329others(7): Show | 10 | HG01255.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.405+853C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683698 | ||||||
chr7:16683715
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.405+870G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683715 | ||||||
chr7:16683858
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.405+1013C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683858 | ||||||
chr7:16683908
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405+1063T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683908 | ||||||
chr7:16683967
|
A | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+1122A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683967 | ||||||
chr7:16684033
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(161): Show | 167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.405+1188G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684033 | ||||||
chr7:16684084
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.405+1239A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684084 | ||||||
chr7:16684109
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405+1264A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684109 | ||||||
chr7:16684148
|
T | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(151): Show | 157 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.405+1303T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684148 | ||||||
chr7:16684209
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.405+1364C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684209 | ||||||
chr7:16684305
|
A | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(105): Show | 109 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.405+1460A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684305 | ||||||
chr7:16684340
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0002g0363 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.405+1495A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684340 | ||||||
chr7:16684361
|
C | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0273others(13): Show | 16 | HG01255.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+1516C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684361 | ||||||
chr7:16684380
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(105): Show | 109 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.406-1525G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684380 | ||||||
chr7:16684460
|
GTTA | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0194a0001c0001t0001g0201others(4): Show | 7 | HG00621.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-1439_406-1437d others(5): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16684460 | |||||
chr7:16684618
|
A | G | 1 | a0001c0001t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.406-1287A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684618 | ||||||
chr7:16684774
|
G | T | 3 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0001t0002g0389 | 3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.406-1131G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684774 | ||||||
chr7:16684821
|
T | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.406-1084T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684821 | ||||||
chr7:16684902
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.406-1003A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684902 | ||||||
chr7:16684995
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.406-910G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684995 | ||||||
chr7:16685004
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.406-901T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685004 | ||||||
chr7:16685054
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.406-851A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685054 | ||||||
chr7:16685195
|
G | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(106): Show | 110 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.406-710G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685195 | ||||||
chr7:16685206
|
T | C | 1 | a0001c0001t0003g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.406-699T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685206 | ||||||
chr7:16685222
|
A | G | 19 | a0001c0001t0001g0162a0001c0001t0001g0283a0001c0001t0002g0287others(16): Show | 19 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.406-683A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685222 | ||||||
chr7:16685367
|
A | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-538A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685367 | ||||||
chr7:16685401
|
G | A | 6 | a0001c0001t0002g0328a0001c0001t0002g0330a0001c0001t0002g0331others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.406-504G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685401 | ||||||
chr7:16685409
|
C | T | 2 | a0001c0003t0002g0295a0001c0003t0002g0313 | 2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.406-496C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685409 | ||||||
chr7:16685412
|
G | GT | 12 | a0001c0001t0001g0180a0001c0001t0001g0209a0001c0001t0001g0230others(9): Show | 13 | HG00280.hp1 HG01074.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.406-481dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16685412 | |||||
chr7:16685431
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.406-474G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685431 | ||||||
chr7:16685463
|
G | T | 22 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0123others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.406-442G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685463 | ||||||
chr7:16685655
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0002g0363 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.406-250A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685655 | ||||||
chr7:16685761
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.406-144C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685761 | ||||||
chr7:16685842
|
T | C | 1 | a0001c0001t0002g0353 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.406-63T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685842 | ||||||
chr7:16685876
|
C | CT | 122 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(119): Show | 124 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.406-10dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16685876 | |||||
chr7:16685876
|
CT | C | 17 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0143others(14): Show | 17 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.406-10delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16685876 | |||||
chr7:16686121
|
T | C | 1 | a0001c0001t0002g0368 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.541+81T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686121 | ||||||
chr7:16686130
|
T | C | 1 | a0001c0001t0006g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541+90T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686130 | ||||||
chr7:16686228
|
G | T | 2 | a0001c0001t0002g0379a0001c0001t0002g0380 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.541+188G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686228 | ||||||
chr7:16686279
|
A | C | 26 | a0001c0001t0001g0157a0001c0001t0001g0255a0001c0001t0002g0007others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.541+239A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686279 | ||||||
chr7:16686394
|
T | C | 1 | a0001c0001t0002g0012 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.541+354T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686394 | ||||||
chr7:16686527
|
A | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 40 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.541+487A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686527 | ||||||
chr7:16686529
|
T | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(6): Show | 10 | HG01243.hp1 HG02257.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.541+489T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686529 | ||||||
chr7:16686629
|
A | ATT | 3 | a0001c0001t0001g0130a0001c0001t0001g0206a0001c0001t0001g0404 | 3 | HG02523.hp2 NA18939.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.541+590_541+591ins others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16686629 | |||||
chr7:16686712
|
T | C | 1 | a0001c0001t0006g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541+672T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686712 | ||||||
chr7:16686718
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.541+678G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686718 | ||||||
chr7:16686738
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.541+698C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686738 | ||||||
chr7:16686742
|
A | T | 19 | a0001c0001t0001g0162a0001c0001t0001g0283a0001c0001t0002g0287others(16): Show | 19 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.541+702A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686742 | ||||||
chr7:16686998
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.541+958C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686998 | ||||||
chr7:16687006
|
CACACAGA others(6): Show |
C | 2 | a0001c0001t0001g0018a0001c0001t0006g0152 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.541+970_541+982del others(13): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16687006 | |||||
chr7:16687154
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.541+1114C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687154 | ||||||
chr7:16687226
|
A | G | 1 | a0001c0003t0002g0313 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541+1186A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687226 | ||||||
chr7:16687331
|
A | G | 1 | a0001c0001t0008g0317 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.541+1291A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687331 | ||||||
chr7:16687582
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541+1542G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687582 | ||||||
chr7:16687610
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.541+1570G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687610 | ||||||
chr7:16687721
|
A | G | 6 | a0001c0001t0002g0290a0001c0001t0002g0300a0001c0001t0002g0319others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+1681A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687721 | ||||||
chr7:16687723
|
A | T | 30 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0123others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.541+1683A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687723 | ||||||
chr7:16687727
|
A | G | 1 | a0001c0001t0002g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.541+1687A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687727 | ||||||
chr7:16687778
|
C | A | 1 | a0001c0001t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.541+1738C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687778 | ||||||
chr7:16687802
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0013others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+1762G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687802 | ||||||
chr7:16687809
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0006g0152 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.541+1769C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687809 | ||||||
chr7:16687816
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.541+1776G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687816 | ||||||
chr7:16687860
|
A | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(3): Show | 7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+1820A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687860 | ||||||
chr7:16687884
|
C | T | 1 | a0001c0001t0010g0402 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.541+1844C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687884 | ||||||
chr7:16687904
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(88): Show | 93 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.541+1864T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687904 | ||||||
chr7:16687997
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.542-1800G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687997 | ||||||
chr7:16688031
|
G | GT | 6 | a0001c0001t0001g0028a0001c0001t0001g0138a0001c0001t0001g0158others(3): Show | 7 | HG01257.hp2 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-1756dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16688031 | |||||
chr7:16688125
|
A | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG02129.hp2 NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.542-1672A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688125 | ||||||
chr7:16688173
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0002g0333 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.542-1624G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688173 | ||||||
chr7:16688286
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0002g0051 | 2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.542-1511C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688286 | ||||||
chr7:16688426
|
A | G | 25 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0120others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.542-1371A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688426 | ||||||
chr7:16688553
|
G | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0316 | 3 | HG02257.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.542-1244G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688553 | ||||||
chr7:16688559
|
T | G | 4 | a0001c0001t0001g0199a0001c0001t0001g0213a0001c0001t0001g0218others(1): Show | 4 | NA18940.hp2 NA18982.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-1238T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688559 | ||||||
chr7:16688626
|
T | A | 1 | a0001c0001t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-1171T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688626 | ||||||
chr7:16688856
|
A | AT | 35 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(32): Show | 36 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.542-932dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16688856 | |||||
chr7:16688973
|
C | A | 21 | a0001c0001t0001g0162a0001c0001t0001g0283a0001c0001t0002g0013others(18): Show | 21 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.542-824C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688973 | ||||||
chr7:16689127
|
G | A | 1 | a0001c0001t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.542-670G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689127 | ||||||
chr7:16689180
|
C | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.542-617C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689180 | ||||||
chr7:16689292
|
A | G | 1 | a0001c0001t0008g0317 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.542-505A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689292 | ||||||
chr7:16689318
|
A | C | 1 | a0001c0001t0001g0254 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.542-479A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689318 | ||||||
chr7:16689380
|
A | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(10): Show | 14 | HG01109.hp1 HG02257.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.542-417A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689380 | ||||||
chr7:16689470
|
G | A | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(10): Show | 14 | HG01109.hp1 HG02257.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.542-327G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689470 | ||||||
chr7:16689627
|
G | T | 22 | a0001c0001t0001g0162a0001c0001t0001g0283a0001c0001t0002g0013others(19): Show | 22 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.542-170G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689627 | ||||||
chr7:16689636
|
A | T | 1 | a0001c0001t0002g0403 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.542-161A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689636 | ||||||
chr7:16689712
|
A | C | 2 | a0001c0001t0001g0018a0001c0001t0006g0152 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.542-85A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689712 | ||||||
chr7:16689747
|
A | T | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.542-50A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689747 | ||||||
chr7:16689768
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.542-29G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689768 | ||||||
chr7:16690143
|
T | C | 1 | a0001c0006t0002g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.651+237T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690143 | ||||||
chr7:16690195
|
A | G | 6 | a0001c0001t0001g0168a0001c0001t0002g0300a0001c0001t0002g0337others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+289A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690195 | ||||||
chr7:16690207
|
C | CT | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(34): Show | 39 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.651+314dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16690207 | |||||
chr7:16690212
|
T | C | 53 | a0001c0001t0001g0018a0001c0001t0001g0108a0001c0001t0001g0120others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.651+306T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690212 | ||||||
chr7:16690272
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.651+366G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690272 | ||||||
chr7:16690384
|
T | A | 3 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0001t0002g0389 | 3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.651+478T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690384 | ||||||
chr7:16690722
|
C | A | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.651+816C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690722 | ||||||
chr7:16690756
|
T | C | 1 | a0001c0001t0002g0353 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.651+850T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690756 | ||||||
chr7:16690917
|
C | T | 33 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0123others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.651+1011C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690917 | ||||||
chr7:16691217
|
G | T | 14 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0001g0273others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+1311G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691217 | ||||||
chr7:16691219
|
T | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0401 | 3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.651+1313T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691219 | ||||||
chr7:16691417
|
G | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(106): Show | 111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.651+1511G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691417 | ||||||
chr7:16691553
|
G | A | 3 | a0001c0001t0002g0354a0001c0001t0002g0364a0001c0001t0002g0382 | 3 | HG00099.hp2 HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.651+1647G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691553 | ||||||
chr7:16691567
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(32): Show | 36 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.651+1661A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691567 | ||||||
chr7:16691588
|
A | G | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.651+1682A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691588 | ||||||
chr7:16691592
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.651+1686A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691592 | ||||||
chr7:16691602
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0002g0078 | 2 | NA18967.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.651+1696G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691602 | ||||||
chr7:16691628
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(166): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.651+1722A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691628 | ||||||
chr7:16691653
|
C | T | 1 | a0001c0001t0009g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.651+1747C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691653 | ||||||
chr7:16691741
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0249 | 2 | NA18939.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.651+1835A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691741 | ||||||
chr7:16691789
|
A | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0002g0335others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+1883A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691789 | ||||||
chr7:16691878
|
C | CTG | 11 | a0001c0001t0001g0189a0001c0001t0001g0237a0001c0001t0002g0080others(8): Show | 11 | HG00423.hp2 HG01106.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.651+1996_651+1997d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16691878 | |||||
chr7:16691878
|
CTG | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.651+1996_651+1997d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16691878 | |||||
chr7:16691878
|
CTGTG | C | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0001g0204others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+1994_651+1997d others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16691878 | |||||
chr7:16691912
|
G | A | 10 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651+2006G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691912 | ||||||
chr7:16691928
|
A | G | 21 | a0001c0001t0001g0162a0001c0001t0001g0283a0001c0001t0002g0013others(18): Show | 21 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.651+2022A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691928 | ||||||
chr7:16691999
|
C | G | 4 | a0001c0001t0001g0235a0001c0001t0001g0248a0001c0001t0001g0261others(1): Show | 4 | HG02071.hp1 HG02071.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+2093C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691999 | ||||||
chr7:16692236
|
AACCCTTA others(2): Show |
A | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(10): Show | 14 | HG01109.hp1 HG02257.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+2333_651+2341d others(11): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16692236 | |||||
chr7:16692307
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(104): Show | 109 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.651+2401A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692307 | ||||||
chr7:16692460
|
T | A | 10 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-2374T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692460 | ||||||
chr7:16692621
|
G | A | 16 | a0001c0001t0001g0283a0001c0001t0002g0287a0001c0001t0002g0288others(13): Show | 16 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-2213G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692621 | ||||||
chr7:16692734
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0157others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.652-2100G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692734 | ||||||
chr7:16692758
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.652-2076C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692758 | ||||||
chr7:16693231
|
C | T | 1 | a0001c0001t0002g0373 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.652-1603C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693231 | ||||||
chr7:16693354
|
A | G | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.652-1480A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693354 | ||||||
chr7:16693394
|
A | G | 1 | a0001c0001t0002g0323 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.652-1440A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693394 | ||||||
chr7:16693542
|
T | C | 34 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(31): Show | 35 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.652-1292T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693542 | ||||||
chr7:16693606
|
TGCTTTAC others(3): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652-1226_652-1217d others(12): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16693606 | |||||
chr7:16693620
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652-1214A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693620 | ||||||
chr7:16693639
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652-1195T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693639 | ||||||
chr7:16693639
|
T | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(10): Show | 14 | HG01109.hp1 HG02257.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.652-1195T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693639 | ||||||
chr7:16693885
|
A | G | 7 | a0001c0001t0002g0009a0001c0001t0002g0032a0001c0001t0002g0290others(4): Show | 8 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-949A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693885 | ||||||
chr7:16693942
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.652-892G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693942 | ||||||
chr7:16693946
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.652-888C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693946 | ||||||
chr7:16693989
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0296 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.652-845A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693989 | ||||||
chr7:16694186
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | NA18943.hp1 NA18983.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-648A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694186 | ||||||
chr7:16694247
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0372a0001c0001t0002g0373 | 4 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-587G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694247 | ||||||
chr7:16694432
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0205 | 2 | HG01257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.652-402G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694432 | ||||||
chr7:16694434
|
G | T | 1 | a0001c0001t0010g0402 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.652-400G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694434 | ||||||
chr7:16694682
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0021others(95): Show | 100 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.652-152G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694682 | ||||||
chr7:16694800
|
C | A | 10 | a0001c0001t0001g0017a0001c0001t0002g0329a0001c0001t0002g0374others(7): Show | 10 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-34C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694800 | ||||||
chr7:16695017
|
G | A | 6 | a0001c0001t0001g0283a0001c0001t0002g0323a0001c0001t0005g0153others(3): Show | 6 | HG01081.hp2 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+13G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695017 | ||||||
chr7:16695062
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0004g0318 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.822+58G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695062 | ||||||
chr7:16695063
|
C | T | 1 | a0001c0001t0002g0374 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.822+59C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695063 | ||||||
chr7:16695112
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.822+108T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695112 | ||||||
chr7:16695120
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(161): Show | 167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.822+116G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695120 | ||||||
chr7:16695266
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(156): Show | 162 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.822+262A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695266 | ||||||
chr7:16695282
|
A | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.822+278A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695282 | ||||||
chr7:16695347
|
G | T | 1 | a0001c0004t0002g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.822+343G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695347 | ||||||
chr7:16695514
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.822+510T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695514 | ||||||
chr7:16695536
|
A | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0167a0001c0001t0001g0206others(3): Show | 6 | HG02523.hp2 NA18747.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+532A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695536 | ||||||
chr7:16695617
|
C | CT | 9 | a0001c0001t0001g0191a0001c0001t0001g0236a0001c0001t0001g0273others(6): Show | 9 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.822+621dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 16695617 | |||||
chr7:16695646
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(230): Show | 238 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.822+642G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695646 | ||||||
chr7:16695697
|
A | G | 1 | a0001c0002t0003g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.822+693A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695697 | ||||||
chr7:16695705
|
C | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(49): Show | 53 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.822+701C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695705 | ||||||
chr7:16695713
|
C | T | 3 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0001t0002g0389 | 3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.822+709C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695713 | ||||||
chr7:16695923
|
T | G | 351 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(348): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.822+919T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695923 | ||||||
chr7:16695961
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(321): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.823-954T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695961 | ||||||
chr7:16695971
|
G | A | 1 | a0001c0001t0002g0403 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-944G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695971 | ||||||
chr7:16695972
|
T | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0155a0001c0001t0001g0156others(17): Show | 21 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-943T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695972 | ||||||
chr7:16696035
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0237a0001c0001t0002g0072 | 3 | HG00423.hp2 HG02135.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.823-880C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696035 | ||||||
chr7:16696041
|
C | T | 4 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0001t0002g0389others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-874C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696041 | ||||||
chr7:16696114
|
T | G | 4 | a0001c0001t0001g0169a0001c0001t0002g0335a0001c0002t0002g0324others(1): Show | 4 | HG01884.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-801T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696114 | ||||||
chr7:16696135
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0161a0001c0001t0001g0168others(2): Show | 6 | HG02486.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-780G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696135 | ||||||
chr7:16696138
|
AG | A | 8 | a0001c0001t0001g0234a0001c0001t0001g0243a0001c0001t0001g0254others(5): Show | 8 | NA18945.hp1 NA18956.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-774delG | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 16696138 | |||||
chr7:16696141
|
G | A | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(117): Show | 124 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.823-774G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696141 | ||||||
chr7:16696157
|
C | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0029others(74): Show | 80 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.823-758C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696157 | ||||||
chr7:16696178
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-737G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696178 | ||||||
chr7:16696191
|
G | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0029others(21): Show | 24 | HG00099.hp2 HG00558.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.823-724G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696191 | ||||||
chr7:16696192
|
A | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(229): Show | 239 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.823-723A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696192 | ||||||
chr7:16696199
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.823-716T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696199 | ||||||
chr7:16696207
|
T | C | 6 | a0001c0001t0002g0289a0001c0001t0002g0326a0001c0001t0002g0335others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-708T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696207 | ||||||
chr7:16696268
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.823-647T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696268 | ||||||
chr7:16696388
|
A | G | 4 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0001t0002g0389others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-527A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696388 | ||||||
chr7:16696436
|
A | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0108others(50): Show | 55 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.823-479A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696436 | ||||||
chr7:16696542
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0203a0001c0001t0001g0252others(1): Show | 4 | NA18972.hp1 NA18978.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-373T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696542 | ||||||
chr7:16696544
|
G | GA | 117 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0028others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.823-371_823-370ins others(1): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696544 | ||||||
chr7:16696561
|
G | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.823-354G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696561 | ||||||
chr7:16696718
|
T | TA | 42 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0113others(39): Show | 43 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.823-192dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 16696718 | |||||
chr7:16696720
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.823-195A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696720 | ||||||
chr7:16696754
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.823-161T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696754 | ||||||
chr7:16696780
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.823-135T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696780 | ||||||
chr7:16696853
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0168others(23): Show | 27 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.823-62G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696853 | ||||||
chr7:16696854
|
C | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.823-61C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696854 | ||||||
chr7:16697113
|
T | TTTTG | 27 | a0001c0001t0001g0015a0001c0001t0001g0155a0001c0001t0001g0156others(24): Show | 28 | HG01074.hp2 HG01109.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.969+73_969+76dupTT others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 16697113 | |||||
chr7:16697265
|
T | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0027others(106): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.969+204T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697265 | ||||||
chr7:16697288
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0235a0001c0001t0001g0248others(2): Show | 5 | HG00609.hp2 HG02071.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.969+227G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697288 | ||||||
chr7:16697299
|
C | G | 3 | a0001c0001t0002g0331a0001c0001t0002g0333a0001c0001t0002g0338 | 3 | HG01109.hp1 HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.969+238C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697299 | ||||||
chr7:16697361
|
A | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0001g0180others(16): Show | 19 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+300A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697361 | ||||||
chr7:16697377
|
A | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0001g0180others(16): Show | 19 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+316A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697377 | ||||||
chr7:16697487
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.969+426C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697487 | ||||||
chr7:16697710
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.970-338C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697710 | ||||||
chr7:16697995
|
G | T | 5 | a0001c0001t0003g0282a0001c0002t0002g0292a0001c0002t0002g0324others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.970-53G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697995 | ||||||
chr7:16698363
|
G | A | 1 | a0001c0001t0010g0402 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1108+177G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698363 | ||||||
chr7:16698374
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1108+188G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698374 | ||||||
chr7:16698381
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0027others(97): Show | 102 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1108+195T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698381 | ||||||
chr7:16698414
|
A | G | 8 | a0001c0001t0001g0162a0001c0001t0002g0319a0001c0001t0002g0323others(5): Show | 8 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108+228A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698414 | ||||||
chr7:16698454
|
A | G | 44 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0031others(41): Show | 45 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1108+268A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698454 | ||||||
chr7:16698460
|
A | C | 5 | a0001c0001t0001g0255a0001c0001t0002g0051a0001c0001t0002g0354others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+274A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698460 | ||||||
chr7:16698670
|
A | G | 37 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0031others(34): Show | 38 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1108+484A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698670 | ||||||
chr7:16698671
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1108+485G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698671 | ||||||
chr7:16698776
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1108+590A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698776 | ||||||
chr7:16699292
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1108+1106T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699292 | ||||||
chr7:16699322
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1108+1136A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699322 | ||||||
chr7:16699469
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 64 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1108+1283C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699469 | ||||||
chr7:16699538
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1108+1352G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699538 | ||||||
chr7:16699592
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1108+1406C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699592 | ||||||
chr7:16699696
|
A | C | 1 | a0001c0001t0002g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1108+1510A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699696 | ||||||
chr7:16699725
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(275): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1108+1539A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699725 | ||||||
chr7:16699784
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0002g0319a0001c0001t0002g0328others(2): Show | 5 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+1598G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699784 | ||||||
chr7:16699859
|
T | C | 1 | a0001c0001t0002g0329 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1108+1673T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699859 | ||||||
chr7:16699946
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1108+1760A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699946 | ||||||
chr7:16700078
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1108+1892T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700078 | ||||||
chr7:16700308
|
G | A | 5 | a0001c0001t0001g0174a0001c0001t0002g0001a0001c0001t0002g0077others(2): Show | 8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108+2122G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700308 | ||||||
chr7:16700344
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1108+2158T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700344 | ||||||
chr7:16700422
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0002g0378 | 2 | NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1108+2236T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700422 | ||||||
chr7:16700476
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(268): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1108+2290G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700476 | ||||||
chr7:16700517
|
A | G | 1 | a0001c0001t0002g0397 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1108+2331A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700517 | ||||||
chr7:16700759
|
A | G | 13 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0284others(10): Show | 14 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1108+2573A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700759 | ||||||
chr7:16700824
|
G | A | 3 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0007t0002g0336 | 3 | HG01243.hp2 HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1108+2638G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700824 | ||||||
chr7:16700929
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0027others(102): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1108+2743A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700929 | ||||||
chr7:16701077
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0284a0001c0001t0002g0012others(1): Show | 5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+2891A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701077 | ||||||
chr7:16701526
|
A | G | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1109-3021A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701526 | ||||||
chr7:16701530
|
C | G | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1109-3017C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701530 | ||||||
chr7:16701655
|
T | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0027others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1109-2892T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701655 | ||||||
chr7:16701659
|
C | CTA | 6 | a0001c0001t0001g0255a0001c0001t0002g0051a0001c0001t0002g0354others(3): Show | 6 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-2888_1109-288 others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701659 | ||||||
chr7:16701850
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1109-2697A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701850 | ||||||
chr7:16702075
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1109-2472C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702075 | ||||||
chr7:16702391
|
C | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0155a0001c0001t0001g0156others(17): Show | 20 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-2156C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702391 | ||||||
chr7:16702419
|
C | T | 3 | a0001c0001t0002g0332a0001c0001t0002g0376a0001c0007t0002g0336 | 3 | HG01243.hp2 HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1109-2128C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702419 | ||||||
chr7:16702507
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1109-2040G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702507 | ||||||
chr7:16702510
|
C | T | 3 | a0001c0001t0002g0321a0001c0001t0002g0388a0001c0003t0002g0320 | 3 | HG02145.hp1 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1109-2037C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702510 | ||||||
chr7:16702606
|
T | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0155a0001c0001t0001g0156others(18): Show | 21 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1109-1941T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702606 | ||||||
chr7:16702840
|
T | C | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1109-1707T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702840 | ||||||
chr7:16702996
|
G | A | 4 | a0001c0001t0002g0332a0001c0001t0002g0335a0001c0001t0002g0376others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-1551G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702996 | ||||||
chr7:16703114
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1109-1433C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703114 | ||||||
chr7:16703230
|
C | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0284a0001c0001t0002g0012others(1): Show | 5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-1317C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703230 | ||||||
chr7:16703332
|
A | G | 1 | a0001c0001t0007g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1109-1215A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703332 | ||||||
chr7:16703571
|
T | C | 1 | a0001c0001t0002g0392 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1109-976T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703571 | ||||||
chr7:16703865
|
C | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0165a0001c0001t0002g0082others(3): Show | 6 | HG01952.hp2 HG02602.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-682C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703865 | ||||||
chr7:16704090
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0038a0001c0001t0002g0043others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-457T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16704090 | ||||||
chr7:16704413
|
G | C | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1109-134G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16704413 | ||||||
chr7:16704528
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1109-19C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16704528 | ||||||
chr7:16704746
|
G | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0241 | 2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1231+77G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704746 | ||||||
chr7:16704791
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1231+122G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704791 | ||||||
chr7:16704800
|
A | C | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1231+131A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704800 | ||||||
chr7:16704884
|
T | G | 2 | a0001c0001t0002g0403a0001c0001t0010g0402 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1231+215T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704884 | ||||||
chr7:16705144
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0027others(94): Show | 99 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1231+475G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705144 | ||||||
chr7:16705236
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1231+567G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705236 | ||||||
chr7:16705258
|
G | C | 20 | a0001c0001t0001g0015a0001c0001t0001g0155a0001c0001t0001g0156others(17): Show | 20 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231+589G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705258 | ||||||
chr7:16705307
|
AAG | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0027others(93): Show | 98 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1231+640_1231+641d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 16705307 | |||||
chr7:16705457
|
G | A | 1 | a0001c0001t0002g0374 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1232-603G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705457 | ||||||
chr7:16705610
|
A | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(329): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1232-450A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705610 | ||||||
chr7:16705684
|
C | CA | 30 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(27): Show | 30 | HG00738.hp1 HG01074.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1232-358dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 16705684 | |||||
chr7:16705746
|
A | G | 1 | a0001c0003t0002g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1232-314A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705746 | ||||||
chr7:16705803
|
A | G | 7 | a0001c0001t0001g0162a0001c0001t0002g0319a0001c0001t0002g0331others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1232-257A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705803 | ||||||
chr7:16705939
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0161a0001c0001t0001g0171others(15): Show | 18 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1232-121G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705939 | ||||||
chr7:16705964
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1232-96T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705964 |