geneid | 54849 |
---|---|
ensemblid | ENSG00000140995.17 |
hgncid | 25969 |
symbol | DEF8 |
name | differentially expressed in FDCP 8 homolog |
refseq_nuc | NM_001242818.2 |
refseq_prot | NP_001229747.1 |
ensembl_nuc | ENST00000563594.6 |
ensembl_prot | ENSP00000458019.1 |
mane_status | MANE Select |
chr | chr16 |
start | 89948755 |
end | 89968060 |
strand | + |
ver | v1.2 |
region | chr16:89948755-89968060 |
region5000 | chr16:89943755-89973060 |
regionname0 | DEF8_chr16_89948755_89968060 |
regionname5000 | DEF8_chr16_89943755_89973060 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 451 | 377 | 88 | 74 | 148 | 18 | 47 | 118 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0002 | 0/0 | 451 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0003 | 0/0 | 451 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0004 | 0/0 | 268 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1356 | 328 | 50 | 70 | 148 | 17 | 41 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0002 | 0/0 | 1356 | 40 | 30 | 3 | 0 | 1 | 6 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0003 | 0/0 | 1356 | 7 | 6 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0004 | 0/0 | 1356 | 7 | 7 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0005 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0006 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0007 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0008 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
c0009 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2265 | 270 | 52 | 55 | 119 | 12 | 31 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0002 | 0/0 | 2265 | 30 | 0 | 1 | 29 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0003 | 0/0 | 2265 | 14 | 0 | 6 | 0 | 0 | 8 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0004 | 1/0 | 2265 | 10 | 1 | 4 | 0 | 4 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0005 | 0/0 | 2265 | 10 | 2 | 1 | 0 | 0 | 7 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0006 | 0/0 | 2265 | 8 | 8 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0007 | 0/0 | 2265 | 7 | 6 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0008 | 0/0 | 2265 | 6 | 5 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0009 | 0/0 | 2265 | 5 | 5 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0010 | 0/0 | 2265 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0011 | 0/0 | 2265 | 4 | 3 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0012 | 0/0 | 2265 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0013 | 0/0 | 2265 | 3 | 0 | 2 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0014 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0015 | 0/0 | 2265 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0016 | 0/0 | 2265 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0017 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0018 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0019 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0020 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0021 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0022 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0023 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0024 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0025 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0026 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
t0027 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 33 | 0 | 12 | 18 | 1 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0002 | 0/0 | 23 | 0 | 6 | 9 | 4 | 4 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0003 | 0/0 | 17 | 0 | 1 | 16 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0004 | 0/0 | 16 | 0 | 5 | 11 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0005 | 1/1 | 8 | 0 | 0 | 6 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0007 | 0/0 | 6 | 0 | 2 | 0 | 3 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0019 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0039 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1356 | 328 | 50 | 70 | 148 | 17 | 41 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002 | 0/0 | 1356 | 40 | 30 | 3 | 0 | 1 | 6 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0003 | 0/0 | 1356 | 7 | 6 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0008 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0009 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0002c0004 | 0/0 | 1356 | 7 | 7 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0002c0005 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0003c0006 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0004c0007 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3620 | 257 | 42 | 54 | 117 | 12 | 31 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0002 | 0/0 | 3620 | 30 | 0 | 1 | 29 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0003 | 0/0 | 3620 | 14 | 0 | 6 | 0 | 0 | 8 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0004 | 1/0 | 3620 | 10 | 1 | 4 | 0 | 4 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0010 | 0/0 | 3620 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0013 | 0/0 | 3620 | 3 | 0 | 2 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0015 | 0/0 | 3620 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0016 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0018 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0019 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0020 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0021 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0023 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0001t0027 | 0/0 | 3620 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0001 | 0/0 | 3620 | 4 | 3 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0005 | 0/0 | 3620 | 8 | 1 | 1 | 0 | 0 | 6 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0006 | 0/0 | 3620 | 8 | 8 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0007 | 0/0 | 3620 | 6 | 5 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0011 | 0/0 | 3620 | 4 | 3 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0012 | 0/0 | 3620 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0014 | 0/0 | 3620 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0017 | 0/0 | 3620 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0024 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0025 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0002t0026 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0003t0007 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0003t0008 | 0/0 | 3620 | 6 | 5 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0008t0005 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0001c0009t0022 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0002c0004t0001 | 0/0 | 3620 | 7 | 7 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0002c0005t0009 | 0/0 | 3620 | 5 | 5 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0003c0006t0001 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
a0004c0007t0005 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | copy fasta | chr16 | 89943755 | 89973060 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 0 | 12 | 18 | 1 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0002 | 0/0 | 21 | 0 | 5 | 9 | 3 | 4 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0004 | 0/0 | 15 | 0 | 5 | 10 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0005 | 0/1 | 7 | 0 | 0 | 6 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 0 | 3 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0019 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0039 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0003 | 0/0 | 17 | 0 | 1 | 16 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0004g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0004g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0010g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0013g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0015g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0016g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0016g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0019g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0021g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0001t0027g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0005g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0005g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0007g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0011g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0017g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0024g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0025g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0002t0026g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0003t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0008t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0001c0009t0022g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0004t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0005t0009g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0005t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0002c0005t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0003c0006t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0003c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
a0004c0007t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0013 | g0038 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00099 | hp2 | a0001 | c0002 | t0011 | g0078 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0063 | EUR | GBR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00639 | hp1 | a0001 | c0002 | t0005 | g0046 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00733 | hp2 | a0001 | c0001 | t0027 | g0059 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01069 | hp2 | a0001 | c0001 | t0015 | g0024 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01071 | hp1 | a0001 | c0001 | t0015 | g0024 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01081 | hp2 | a0001 | c0003 | t0008 | g0211 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01109 | hp2 | a0001 | c0002 | t0007 | g0114 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01358 | hp1 | a0001 | c0001 | t0013 | g0038 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01433 | hp2 | a0001 | c0001 | t0013 | g0193 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01884 | hp1 | a0001 | c0008 | t0005 | g0084 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01891 | hp2 | a0001 | c0003 | t0008 | g0076 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02015 | hp2 | a0001 | c0001 | t0016 | g0186 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02055 | hp1 | a0001 | c0003 | t0007 | g0179 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02055 | hp2 | a0002 | c0005 | t0009 | g0223 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02145 | hp1 | a0001 | c0001 | t0019 | g0177 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02145 | hp2 | a0002 | c0005 | t0009 | g0096 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02257 | hp2 | a0002 | c0004 | t0001 | g0220 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02258 | hp1 | a0001 | c0001 | t0010 | g0079 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0048 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02280 | hp2 | a0001 | c0002 | t0007 | g0048 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02451 | hp1 | a0001 | c0002 | t0006 | g0081 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02451 | hp2 | a0002 | c0005 | t0009 | g0022 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0014 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02717 | hp2 | a0001 | c0002 | t0012 | g0071 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02723 | hp1 | a0001 | c0002 | t0026 | g0200 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0061 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02809 | hp2 | a0001 | c0001 | t0020 | g0064 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02818 | hp1 | a0001 | c0002 | t0011 | g0215 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02886 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02886 | hp2 | a0002 | c0004 | t0001 | g0221 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02895 | hp2 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02897 | hp2 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02965 | hp1 | a0001 | c0002 | t0017 | g0082 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0046 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02970 | hp1 | a0001 | c0009 | t0022 | g0210 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02976 | hp1 | a0002 | c0005 | t0009 | g0022 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02976 | hp2 | a0001 | c0002 | t0007 | g0088 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03041 | hp2 | a0001 | c0002 | t0012 | g0065 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03139 | hp1 | a0001 | c0001 | t0023 | g0053 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03139 | hp2 | a0001 | c0002 | t0006 | g0066 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0225 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03209 | hp2 | a0001 | c0002 | t0006 | g0069 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03225 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03225 | hp2 | a0001 | c0002 | t0006 | g0051 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03239 | hp1 | a0001 | c0001 | t0021 | g0107 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03453 | hp1 | a0001 | c0002 | t0007 | g0209 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03486 | hp1 | a0001 | c0002 | t0007 | g0214 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03486 | hp2 | a0001 | c0003 | t0008 | g0178 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03490 | hp1 | a0004 | c0007 | t0005 | g0055 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03516 | hp1 | a0001 | c0002 | t0017 | g0083 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03579 | hp2 | a0001 | c0002 | t0024 | g0212 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03688 | hp1 | a0001 | c0002 | t0005 | g0014 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03927 | hp1 | a0001 | c0001 | t0018 | g0164 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04184 | hp1 | a0001 | c0002 | t0005 | g0060 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04184 | hp2 | a0001 | c0002 | t0005 | g0054 | SAS | BEB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04204 | hp2 | a0001 | c0002 | t0005 | g0014 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | STU | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18906 | hp1 | a0001 | c0002 | t0011 | g0213 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18906 | hp2 | a0001 | c0002 | t0012 | g0070 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18973 | hp1 | a0003 | c0006 | t0001 | g0020 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18973 | hp2 | a0003 | c0006 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19030 | hp1 | a0001 | c0002 | t0014 | g0206 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19043 | hp1 | a0001 | c0002 | t0006 | g0067 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19043 | hp2 | a0001 | c0003 | t0008 | g0224 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19087 | hp1 | a0001 | c0001 | t0016 | g0182 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19240 | hp1 | a0002 | c0005 | t0009 | g0022 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA19240 | hp2 | a0001 | c0002 | t0011 | g0216 | AFR | YRI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20129 | hp1 | a0001 | c0003 | t0008 | g0218 | AFR | ASW | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20129 | hp2 | a0001 | c0002 | t0006 | g0073 | AFR | ASW | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | GIH | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02109 | hp1 | a0001 | c0002 | t0025 | g0072 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02109 | hp2 | a0002 | c0004 | t0001 | g0222 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03471 | hp1 | a0001 | c0003 | t0008 | g0219 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG03471 | hp2 | a0001 | c0002 | t0006 | g0077 | AFR | MSL | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA21309 | hp1 | a0001 | c0002 | t0014 | g0207 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0005 | REF | REF | DEF8_chr16_89943755_89973060 | DEF8 | chr16 | 89943755 | 89973060 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89954337
|
C | G | 1 | a0002 | 12 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.85C>G | p.Gln29Glu | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/13 | 252/3620 | 85/1356 | 29/451 | chr16 | 89954337 | ||
chr16:89961847
|
G | GACTTTGA others(3): Show |
1 | a0004 | 1 | HG03490.hp1 | frameshift_variant&stop_gained | HIGH | c.791_800dupACTTTGAG others(2): Show |
p.Arg268fs | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 8/13 | 968/3620 | 801/1356 | 267/451 | INFO_REALIGN_3_PRIME | chr16 | 89961847 | |
chr16:89962072
|
C | T | 1 | a0003 | 2 | NA18973.hp1 NA18973.hp2 |
missense_variant | MODERATE | c.868C>T | p.Arg290Trp | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/13 | 1035/3620 | 868/1356 | 290/451 | chr16 | 89962072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89957577
|
C | T | 1 | a0001c0009 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.289C>T | p.Leu97Leu | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/13 | 456/3620 | 289/1356 | 97/451 | chr16 | 89957577 | ||
chr16:89957654
|
G | A | 1 | a0001c0003 | 7 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
synonymous_variant | LOW | c.366G>A | p.Glu122Glu | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/13 | 533/3620 | 366/1356 | 122/451 | chr16 | 89957654 | ||
chr16:89963395
|
G | A | 1 | a0001c0008 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.954G>A | p.Pro318Pro | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/13 | 1121/3620 | 954/1356 | 318/451 | chr16 | 89963395 | ||
chr16:89965888
|
T | G | 5 | a0001c0002a0001c0003a0001c0008others(2): Show | 54 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(51): Show |
synonymous_variant | LOW | c.1281T>G | p.Thr427Thr | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1448/3620 | 1281/1356 | 427/451 | chr16 | 89965888 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89948768
|
C | G | 1 | a0001c0001t0027 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-154C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/13 | 5485 | chr16 | 89948768 | |||||
chr16:89948793
|
A | G | 3 | a0001c0001t0002a0001c0001t0016a0001c0002t0017 | 34 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-129A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/13 | 5460 | chr16 | 89948793 | |||||
chr16:89966025
|
G | C | 1 | a0001c0002t0014 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*62G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 62 | chr16 | 89966025 | |||||
chr16:89966038
|
C | T | 1 | a0001c0003t0008 | 6 | HG01081.hp2 HG01891.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*75C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 75 | chr16 | 89966038 | |||||
chr16:89966047
|
C | T | 1 | a0001c0001t0013 | 3 | HG00099.hp1 HG01358.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*84C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 84 | chr16 | 89966047 | |||||
chr16:89966147
|
C | T | 12 | a0001c0002t0005a0001c0002t0006a0001c0002t0007others(9): Show | 43 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*184C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 184 | chr16 | 89966147 | |||||
chr16:89966149
|
G | T | 15 | a0001c0002t0005a0001c0002t0006a0001c0002t0007others(12): Show | 50 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*186G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 186 | chr16 | 89966149 | |||||
chr16:89966285
|
C | T | 2 | a0001c0002t0011a0001c0002t0017 | 6 | HG00099.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 322 | chr16 | 89966285 | |||||
chr16:89966328
|
C | A | 1 | a0001c0001t0018 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 365 | chr16 | 89966328 | |||||
chr16:89966368
|
A | G | 3 | a0001c0002t0011a0001c0002t0017a0001c0002t0024 | 7 | HG00099.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 405 | chr16 | 89966368 | |||||
chr16:89966433
|
G | A | 1 | a0001c0001t0010 | 4 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 470 | chr16 | 89966433 | |||||
chr16:89966454
|
G | T | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*491G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 491 | chr16 | 89966454 | |||||
chr16:89966634
|
C | T | 1 | a0001c0002t0026 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 671 | chr16 | 89966634 | |||||
chr16:89966825
|
C | T | 3 | a0001c0002t0011a0001c0002t0017a0001c0002t0024 | 7 | HG00099.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*862C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 862 | chr16 | 89966825 | |||||
chr16:89966847
|
C | G | 11 | a0001c0002t0005a0001c0002t0006a0001c0002t0007others(8): Show | 40 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*884C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 884 | chr16 | 89966847 | |||||
chr16:89967030
|
G | A | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(22): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1067 | chr16 | 89967030 | |||||
chr16:89967038
|
G | A | 1 | a0001c0001t0015 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1075 | chr16 | 89967038 | |||||
chr16:89967112
|
G | A | 1 | a0001c0001t0019 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1149G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1149 | chr16 | 89967112 | |||||
chr16:89967113
|
G | A | 1 | a0001c0002t0006 | 8 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1150G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1150 | chr16 | 89967113 | |||||
chr16:89967422
|
C | G | 12 | a0001c0002t0005a0001c0002t0006a0001c0002t0007others(9): Show | 41 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1459C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1459 | chr16 | 89967422 | |||||
chr16:89967500
|
G | T | 1 | a0001c0001t0021 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1537G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1537 | chr16 | 89967500 | |||||
chr16:89967502
|
C | A | 13 | a0001c0002t0005a0001c0002t0006a0001c0002t0007others(10): Show | 46 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1539C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1539 | chr16 | 89967502 | |||||
chr16:89967640
|
C | G | 1 | a0001c0001t0023 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1677 | chr16 | 89967640 | |||||
chr16:89967709
|
A | G | 4 | a0001c0001t0002a0001c0002t0011a0001c0002t0017others(1): Show | 37 | HG00099.hp2 HG00438.hp2 HG01175.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1746A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 1746 | chr16 | 89967709 | |||||
chr16:89967970
|
G | C | 3 | a0001c0001t0010a0001c0001t0020a0001c0009t0022 | 6 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2007G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 2007 | chr16 | 89967970 | |||||
chr16:89968050
|
T | C | 3 | a0001c0002t0007a0001c0002t0026a0001c0003t0007 | 8 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2087T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 13/13 | 2087 | chr16 | 89968050 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89948824
|
GCGGGGCC others(143): Show |
G | 8 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(5): Show | 9 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+25_-108+174de others(1): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948824 | |||||
chr16:89948824
|
GCGGGGCC others(188): Show |
G | 2 | a0001c0002t0017g0082a0001c0002t0017g0083 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-108+25_-108+219de others(1): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948824 | |||||
chr16:89948839
|
T | A | 33 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0049others(30): Show | 44 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-108+25T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948839 | ||||||
chr16:89948839
|
T | TCGGGGCC others(8): Show |
1 | a0001c0001t0001g0086 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-108+61_-108+75dup others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | |||||
chr16:89948839
|
TCGGGGCC others(8): Show |
T | 15 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(12): Show | 26 | HG01433.hp2 HG02896.hp1 HG02897.hp1 others(23): Show |
intron_variant | MODIFIER | c.-108+61_-108+75del others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | |||||
chr16:89948839
|
TCGGGGCC others(23): Show |
T | 8 | a0001c0001t0001g0217a0001c0002t0006g0225a0001c0002t0007g0048others(5): Show | 9 | HG02258.hp2 HG02280.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+46_-108+75del others(30): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | |||||
chr16:89948839
|
TCGGGGCC others(38): Show |
T | 1 | a0001c0001t0001g0008 | 5 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108+31_-108+75del others(45): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | |||||
chr16:89948839
|
TCGGGGCC others(68): Show |
T | 5 | a0001c0001t0001g0085a0001c0002t0011g0213a0001c0002t0024g0212others(2): Show | 5 | HG01081.hp2 HG01884.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108+46_-108+120de others(76): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948839 | |||||
chr16:89948850
|
G | GGGGACGG others(98): Show |
1 | a0001c0001t0001g0162 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-108+76_-108+180du others(106): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | |||||
chr16:89948850
|
G | GGGGTCGG others(8): Show |
1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+39_-108+40ins others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | |||||
chr16:89948850
|
GGGGACGG others(53): Show |
G | 3 | a0001c0001t0002g0012a0001c0001t0002g0181a0001c0001t0016g0182 | 6 | HG00438.hp2 HG02083.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108+61_-108+120de others(61): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | |||||
chr16:89948850
|
GGGGACGG others(98): Show |
G | 1 | a0001c0001t0003g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-108+76_-108+180de others(1): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948850 | |||||
chr16:89948854
|
A | T | 30 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0068others(27): Show | 41 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-108+40A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948854 | ||||||
chr16:89948860
|
C | T | 11 | a0001c0001t0001g0049a0001c0002t0007g0209a0001c0002t0011g0078others(8): Show | 16 | HG00099.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-108+46C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948860 | ||||||
chr16:89948861
|
C | T | 30 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0068others(27): Show | 41 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-108+47C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948861 | ||||||
chr16:89948864
|
C | G | 31 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0068others(28): Show | 42 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-108+50C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948864 | ||||||
chr16:89948865
|
G | A | 31 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0068others(28): Show | 42 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-108+51G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948865 | ||||||
chr16:89948865
|
G | GGGGACGG others(53): Show |
1 | a0001c0001t0003g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-108+75_-108+76ins others(60): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | |||||
chr16:89948865
|
G | GGGGACGG others(143): Show |
1 | a0001c0001t0001g0160 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-108+121_-108+270d others(152): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | |||||
chr16:89948865
|
G | GGGGACGG others(23): Show |
1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-108+60_-108+61ins others(30): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | |||||
chr16:89948865
|
G | GGGGTCGG others(8): Show |
1 | a0001c0001t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-108+54_-108+55ins others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | |||||
chr16:89948865
|
GGGGACGG others(38): Show |
G | 3 | a0001c0001t0001g0028a0001c0003t0008g0218a0001c0003t0008g0219 | 4 | HG01261.hp1 HG01358.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108+85_-108+129de others(46): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948865 | |||||
chr16:89948870
|
C | G | 6 | a0001c0001t0001g0047a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 7 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108+56C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948870 | ||||||
chr16:89948874
|
G | T | 3 | a0001c0001t0001g0199a0001c0002t0005g0046a0001c0002t0026g0200 | 4 | HG00639.hp1 HG02723.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108+60G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948874 | ||||||
chr16:89948875
|
C | T | 47 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0044others(44): Show | 76 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-108+61C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948875 | ||||||
chr16:89948876
|
C | T | 7 | a0001c0002t0007g0209a0002c0004t0001g0013a0002c0004t0001g0220others(4): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108+62C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948876 | ||||||
chr16:89948876
|
CGGCGGGG others(23): Show |
C | 1 | a0001c0002t0006g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-108+65_-108+94del others(30): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948876 | |||||
chr16:89948879
|
C | G | 25 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(22): Show | 32 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+65C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948879 | ||||||
chr16:89948880
|
G | A | 25 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(22): Show | 32 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+66G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948880 | ||||||
chr16:89948880
|
GGGGACGG others(68): Show |
G | 1 | a0001c0001t0001g0044 | 2 | NA18998.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-108+76_-108+150de others(76): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948880 | |||||
chr16:89948884
|
A | T | 9 | a0001c0001t0002g0003a0001c0001t0002g0183a0001c0001t0002g0184others(6): Show | 25 | HG01175.hp2 HG02015.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-108+70A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948884 | ||||||
chr16:89948889
|
G | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-108+75G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948889 | ||||||
chr16:89948890
|
T | C | 26 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0180others(23): Show | 48 | HG00639.hp1 HG00741.hp1 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.-108+76T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948890 | ||||||
chr16:89948890
|
TCGGCGGG others(98): Show |
T | 1 | a0001c0002t0005g0014 | 3 | HG02602.hp1 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-108+130_-108+234d others(2): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948890 | |||||
chr16:89948891
|
C | T | 15 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0002g0003others(12): Show | 32 | HG00639.hp1 HG01175.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+77C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948891 | ||||||
chr16:89948894
|
C | G | 15 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0002g0003others(12): Show | 32 | HG00639.hp1 HG01175.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+80C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948894 | ||||||
chr16:89948895
|
G | A | 15 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0002g0003others(12): Show | 32 | HG00639.hp1 HG01175.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108+81G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948895 | ||||||
chr16:89948895
|
GGGGTCGG others(8): Show |
G | 1 | a0001c0002t0007g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-108+85_-108+99del others(15): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948895 | |||||
chr16:89948899
|
T | A | 50 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(47): Show | 75 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(72): Show |
intron_variant | MODIFIER | c.-108+85T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948899 | ||||||
chr16:89948899
|
TCGGGGCT others(38): Show |
T | 3 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0004g0092 | 5 | HG01256.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108+121_-108+165d others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948899 | |||||
chr16:89948905
|
C | T | 24 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(21): Show | 31 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-108+91C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948905 | ||||||
chr16:89948906
|
T | C | 39 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(36): Show | 63 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-108+92T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948906 | ||||||
chr16:89948909
|
G | C | 39 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(36): Show | 63 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-108+95G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948909 | ||||||
chr16:89948910
|
A | AGGGACGG others(8): Show |
1 | a0001c0001t0002g0093 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-108+106_-108+120d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948910 | |||||
chr16:89948910
|
A | G | 39 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(36): Show | 63 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-108+96A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948910 | ||||||
chr16:89948910
|
AGGGACGG others(53): Show |
A | 2 | a0001c0002t0005g0060a0001c0002t0005g0061 | 2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-108+121_-108+180d others(62): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948910 | |||||
chr16:89948910
|
AGGGACGG others(68): Show |
A | 5 | a0001c0001t0003g0015a0001c0001t0003g0025a0001c0001t0004g0009others(2): Show | 11 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.-108+115_-108+189d others(77): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948910 | |||||
chr16:89948914
|
A | T | 18 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(15): Show | 20 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-108+100A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948914 | ||||||
chr16:89948914
|
ACGGGGCC others(188): Show |
A | 1 | a0001c0001t0001g0023 | 2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-108+121_-107-288d others(2): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948914 | |||||
chr16:89948920
|
C | T | 2 | a0001c0001t0003g0052a0001c0002t0006g0081 | 2 | HG00741.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-108+106C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948920 | ||||||
chr16:89948920
|
CCGGCGGG others(8): Show |
C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-108+121_-108+135d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948920 | |||||
chr16:89948921
|
C | T | 26 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(23): Show | 33 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108+107C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948921 | ||||||
chr16:89948924
|
C | G | 26 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(23): Show | 33 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108+110C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948924 | ||||||
chr16:89948925
|
G | A | 26 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(23): Show | 33 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108+111G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948925 | ||||||
chr16:89948929
|
A | T | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+115A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948929 | ||||||
chr16:89948933
|
G | A | 2 | a0001c0001t0001g0085a0001c0008t0005g0084 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-108+119G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948933 | ||||||
chr16:89948935
|
T | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0068others(46): Show | 61 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.-108+121T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948935 | ||||||
chr16:89948935
|
TCGGCGGG others(128): Show |
T | 1 | a0001c0002t0006g0225 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-108+137_-108+271d others(2): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948935 | |||||
chr16:89948936
|
C | T | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+122C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948936 | ||||||
chr16:89948939
|
C | G | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+125C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948939 | ||||||
chr16:89948940
|
G | A | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+126G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948940 | ||||||
chr16:89948940
|
GGGGACGG others(8): Show |
G | 4 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0102others(1): Show | 7 | HG00733.hp1 HG01891.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108+137_-108+151d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948940 | |||||
chr16:89948941
|
G | GGGTCGGG others(158): Show |
1 | a0001c0001t0023g0053 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-108+129_-108+130i others(167): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948941 | |||||
chr16:89948944
|
A | ACGGGGCC others(38): Show |
1 | a0001c0001t0001g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-108+136_-108+137i others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948944 | |||||
chr16:89948944
|
A | ACGGGGCT others(98): Show |
3 | a0001c0001t0001g0040a0001c0001t0001g0158a0001c0001t0001g0159 | 4 | HG01928.hp2 HG02148.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108+187_-108+291d others(107): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948944 | |||||
chr16:89948944
|
A | T | 43 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(40): Show | 65 | HG00438.hp2 HG00741.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.-108+130A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948944 | ||||||
chr16:89948949
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 9 | HG01192.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+135G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948949 | ||||||
chr16:89948950
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 10 | HG00099.hp2 HG01192.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108+136C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948950 | ||||||
chr16:89948951
|
T | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(17): Show | 29 | HG00099.hp2 HG01192.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-108+137T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948951 | ||||||
chr16:89948954
|
G | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(11): Show | 22 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108+140G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948954 | ||||||
chr16:89948955
|
A | AGGGACGG others(8): Show |
1 | a0001c0002t0007g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-108+175_-108+189d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948955 | |||||
chr16:89948955
|
A | AGGGACGG others(23): Show |
1 | a0001c0001t0019g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-108+165_-108+166i others(32): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948955 | |||||
chr16:89948955
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(11): Show | 22 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108+141A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948955 | ||||||
chr16:89948955
|
AGGGACGG others(8): Show |
A | 27 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(24): Show | 57 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-108+175_-108+189d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948955 | |||||
chr16:89948959
|
A | T | 7 | a0001c0001t0003g0050a0002c0004t0001g0013a0002c0004t0001g0220others(4): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108+145A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948959 | ||||||
chr16:89948965
|
C | T | 21 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(18): Show | 23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-108+151C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948965 | ||||||
chr16:89948966
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0094others(6): Show | 13 | HG01192.hp1 HG02145.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-108+152C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948966 | ||||||
chr16:89948966
|
CGGCGGGG others(83): Show |
C | 5 | a0001c0001t0001g0217a0001c0002t0007g0048a0001c0002t0007g0214others(2): Show | 6 | HG02258.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108+155_-108+244d others(92): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948966 | |||||
chr16:89948969
|
C | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0044others(28): Show | 37 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.-108+155C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948969 | ||||||
chr16:89948970
|
G | A | 31 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0044others(28): Show | 37 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.-108+156G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948970 | ||||||
chr16:89948970
|
G | GGGGACGG others(38): Show |
1 | a0001c0001t0001g0090 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-108+181_-108+225d others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948970 | |||||
chr16:89948970
|
G | GGGGACGG others(83): Show |
1 | a0001c0001t0001g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-108+180_-108+181i others(92): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948970 | |||||
chr16:89948970
|
G | GGGGACGG others(23): Show |
1 | a0001c0001t0001g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-108+165_-108+166i others(32): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948970 | |||||
chr16:89948974
|
A | T | 2 | a0001c0001t0003g0052a0001c0001t0023g0053 | 2 | HG00741.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-108+160A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948974 | ||||||
chr16:89948980
|
C | T | 16 | a0001c0001t0001g0100a0001c0001t0001g0180a0001c0001t0001g0199others(13): Show | 22 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108+166C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948980 | ||||||
chr16:89948980
|
CCGGCGGG others(53): Show |
C | 1 | a0001c0001t0018g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-108+175_-108+234d others(62): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948980 | |||||
chr16:89948989
|
A | ACGGGGCC others(8): Show |
1 | a0001c0001t0003g0052 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-108+186_-108+187i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948989 | |||||
chr16:89948989
|
A | T | 31 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0001g0202others(28): Show | 54 | HG00099.hp2 HG00639.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.-108+175A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948989 | ||||||
chr16:89948989
|
ACGGGGCC others(8): Show |
A | 2 | a0001c0001t0001g0100a0001c0001t0001g0161 | 2 | HG02080.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-108+182_-108+196d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89948989 | |||||
chr16:89948995
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0085a0001c0001t0001g0094others(16): Show | 25 | HG00438.hp2 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-108+181C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948995 | ||||||
chr16:89948996
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-108+182C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948996 | ||||||
chr16:89948996
|
C | T | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+182C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948996 | ||||||
chr16:89948999
|
C | G | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+185C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89948999 | ||||||
chr16:89949000
|
G | A | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+186G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949000 | ||||||
chr16:89949004
|
T | A | 18 | a0001c0001t0001g0105a0001c0001t0001g0180a0001c0001t0001g0199others(15): Show | 24 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-108+190T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949004 | ||||||
chr16:89949004
|
TCGGGGCT others(68): Show |
T | 13 | a0001c0001t0002g0003a0001c0001t0002g0093a0001c0001t0002g0183others(10): Show | 30 | HG01175.hp2 HG02015.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.-108+197_-108+271d others(77): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949004 | |||||
chr16:89949010
|
C | T | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+196C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949010 | ||||||
chr16:89949011
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 33 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.-108+197T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949011 | ||||||
chr16:89949014
|
G | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 32 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-108+200G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949014 | ||||||
chr16:89949015
|
A | AGGGACGG others(8): Show |
2 | a0001c0001t0001g0017a0001c0003t0008g0211 | 4 | HG01081.hp2 HG01891.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108+211_-108+225d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949015 | |||||
chr16:89949015
|
A | AGGGACGG others(173): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0204a0001c0001t0001g0205 | 4 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108+225_-108+226i others(182): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949015 | |||||
chr16:89949015
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 32 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-108+201A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949015 | ||||||
chr16:89949015
|
AGGGACGG others(53): Show |
A | 1 | a0001c0003t0008g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-108+226_-108+285d others(62): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949015 | |||||
chr16:89949025
|
C | T | 14 | a0001c0001t0003g0015a0001c0001t0003g0025a0001c0001t0003g0050others(11): Show | 21 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-108+211C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949025 | ||||||
chr16:89949027
|
G | A | 3 | a0001c0001t0001g0180a0001c0003t0007g0179a0001c0003t0008g0178 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-108+213G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949027 | ||||||
chr16:89949030
|
G | GGGGTCGG others(8): Show |
1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-108+219_-108+220i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949030 | |||||
chr16:89949030
|
GGGGACGG others(23): Show |
G | 8 | a0001c0001t0001g0085a0001c0001t0020g0064a0001c0002t0006g0066others(5): Show | 8 | HG01884.hp1 HG02809.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108+226_-108+255d others(32): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949030 | |||||
chr16:89949034
|
A | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(20): Show | 25 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-108+220A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949034 | ||||||
chr16:89949040
|
T | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0047others(42): Show | 59 | HG00438.hp2 HG00639.hp1 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.-108+226T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949040 | ||||||
chr16:89949041
|
C | T | 8 | a0001c0001t0001g0180a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 9 | HG00639.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+227C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949041 | ||||||
chr16:89949044
|
C | G | 8 | a0001c0001t0001g0180a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 9 | HG00639.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+230C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949044 | ||||||
chr16:89949045
|
G | A | 8 | a0001c0001t0001g0180a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 9 | HG00639.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+231G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949045 | ||||||
chr16:89949049
|
T | A | 12 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0001g0202others(9): Show | 16 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-108+235T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949049 | ||||||
chr16:89949049
|
TCGGGGCT others(8): Show |
T | 13 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0074others(10): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-108+242_-108+256d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949049 | |||||
chr16:89949056
|
T | C | 15 | a0001c0001t0001g0068a0001c0001t0001g0180a0001c0001t0001g0199others(12): Show | 19 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108+242T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949056 | ||||||
chr16:89949059
|
G | C | 15 | a0001c0001t0001g0068a0001c0001t0001g0180a0001c0001t0001g0199others(12): Show | 19 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108+245G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949059 | ||||||
chr16:89949060
|
A | AGGGACGG others(9): Show |
1 | a0001c0001t0001g0205 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-108+249_-108+264d others(18): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949060 | |||||
chr16:89949060
|
A | G | 15 | a0001c0001t0001g0068a0001c0001t0001g0180a0001c0001t0001g0199others(12): Show | 19 | HG00438.hp2 HG00639.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108+246A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949060 | ||||||
chr16:89949060
|
AGGGACGG others(8): Show |
A | 8 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 9 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108+277_-108+291d others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949060 | |||||
chr16:89949064
|
A | ACGGGGCC others(113): Show |
1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-108+264_-108+265i others(122): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949064 | |||||
chr16:89949064
|
A | T | 10 | a0001c0001t0001g0068a0001c0001t0001g0199a0001c0001t0002g0012others(7): Show | 13 | HG00438.hp2 HG02083.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-108+250A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949064 | ||||||
chr16:89949064
|
ACGGGGCC others(38): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-108+272_-107-287d others(47): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949064 | |||||
chr16:89949079
|
A | ACGGGGCC others(8): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0199 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-108+276_-108+277i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949079 | |||||
chr16:89949079
|
A | ACGGGGCC others(8): Show |
20 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0094others(17): Show | 30 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-108+279_-108+280i others(17): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 89949079 | |||||
chr16:89949079
|
A | T | 54 | a0001c0001t0001g0026a0001c0001t0001g0074a0001c0001t0001g0085others(51): Show | 68 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-108+265A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949079 | ||||||
chr16:89949100
|
C | T | 2 | a0001c0002t0017g0082a0001c0002t0017g0083 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-108+286C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949100 | ||||||
chr16:89949106
|
A | G | 3 | a0001c0002t0017g0082a0001c0002t0017g0083a0001c0003t0008g0224 | 3 | HG02965.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-108+292A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949106 | ||||||
chr16:89949109
|
T | A | 3 | a0001c0002t0017g0082a0001c0002t0017g0083a0001c0003t0008g0224 | 3 | HG02965.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-108+295T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949109 | ||||||
chr16:89949162
|
C | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0094others(17): Show | 25 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-107-255C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949162 | ||||||
chr16:89949171
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0217a0001c0002t0007g0048others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-107-246G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949171 | ||||||
chr16:89949357
|
C | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0156a0001c0001t0003g0015others(11): Show | 22 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-107-60C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949357 | ||||||
chr16:89949388
|
C | T | 2 | a0001c0002t0014g0206a0001c0002t0014g0207 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-107-29C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 1/12 | chr16 | 89949388 | ||||||
chr16:89949552
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0003g0106a0001c0001t0021g0107 | 4 | HG00323.hp1 HG01099.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+39G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949552 | ||||||
chr16:89949737
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11+224G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949737 | ||||||
chr16:89949820
|
C | G | 15 | a0001c0001t0001g0155a0001c0001t0001g0176a0001c0001t0002g0003others(12): Show | 34 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+307C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949820 | ||||||
chr16:89949913
|
G | C | 4 | a0001c0001t0001g0085a0001c0002t0011g0213a0001c0002t0024g0212others(1): Show | 4 | HG01884.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+400G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949913 | ||||||
chr16:89949915
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-11+402C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949915 | ||||||
chr16:89949929
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-11+416A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949929 | ||||||
chr16:89949998
|
C | T | 4 | a0001c0003t0008g0076a0001c0003t0008g0218a0001c0003t0008g0219others(1): Show | 4 | HG01891.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+485C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89949998 | ||||||
chr16:89950007
|
G | C | 1 | a0001c0001t0002g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+494G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950007 | ||||||
chr16:89950016
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-11+503C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950016 | ||||||
chr16:89950217
|
C | G | 10 | a0001c0003t0008g0076a0001c0003t0008g0218a0001c0003t0008g0219others(7): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+704C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950217 | ||||||
chr16:89950303
|
C | G | 2 | a0001c0002t0006g0066a0001c0002t0006g0067 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+790C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950303 | ||||||
chr16:89950390
|
A | AT | 6 | a0001c0001t0001g0039a0001c0001t0001g0151a0001c0001t0001g0175others(3): Show | 7 | HG02809.hp2 HG03540.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+893dupT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89950390 | |||||
chr16:89950390
|
AT | A | 56 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0026others(53): Show | 88 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-11+893delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89950390 | |||||
chr16:89950481
|
C | T | 1 | a0001c0002t0006g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-11+968C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950481 | ||||||
chr16:89950574
|
C | T | 12 | a0001c0001t0003g0075a0001c0002t0006g0051a0001c0002t0006g0066others(9): Show | 12 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+1061C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950574 | ||||||
chr16:89950578
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-11+1065C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950578 | ||||||
chr16:89950786
|
CCT | C | 31 | a0001c0001t0001g0023a0001c0001t0003g0015a0001c0001t0003g0025others(28): Show | 41 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-11+1274_-11+1275d others(4): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950786 | ||||||
chr16:89950791
|
G | C | 1 | a0001c0002t0006g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+1278G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950791 | ||||||
chr16:89950792
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11+1279C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89950792 | ||||||
chr16:89951039
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-11+1526G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951039 | ||||||
chr16:89951073
|
T | C | 2 | a0001c0002t0007g0088a0001c0002t0007g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-11+1560T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951073 | ||||||
chr16:89951260
|
CT | C | 6 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0197others(3): Show | 6 | HG01081.hp2 HG02896.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+1759delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89951260 | |||||
chr16:89951261
|
T | C | 1 | a0001c0001t0001g0011 | 4 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1748T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951261 | ||||||
chr16:89951305
|
G | A | 1 | a0001c0002t0006g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-11+1792G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951305 | ||||||
chr16:89951403
|
C | G | 1 | a0001c0001t0021g0107 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+1890C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951403 | ||||||
chr16:89951425
|
G | T | 1 | a0002c0005t0009g0223 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+1912G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951425 | ||||||
chr16:89951434
|
G | A | 28 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0003g0015others(25): Show | 37 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-11+1921G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951434 | ||||||
chr16:89951481
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-11+1968G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951481 | ||||||
chr16:89951503
|
C | A | 3 | a0001c0001t0001g0180a0001c0003t0007g0179a0001c0003t0008g0178 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-11+1990C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951503 | ||||||
chr16:89951550
|
G | A | 34 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0115others(31): Show | 45 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11+2037G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951550 | ||||||
chr16:89951569
|
G | A | 2 | a0001c0003t0008g0211a0001c0003t0008g0224 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-11+2056G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951569 | ||||||
chr16:89951577
|
C | A | 26 | a0001c0001t0001g0023a0001c0001t0003g0015a0001c0001t0003g0025others(23): Show | 34 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+2064C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951577 | ||||||
chr16:89951577
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+2064C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951577 | ||||||
chr16:89951603
|
G | A | 3 | a0002c0004t0001g0013a0002c0004t0001g0220a0002c0004t0001g0221 | 6 | HG02257.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2090G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951603 | ||||||
chr16:89951664
|
C | T | 29 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 37 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-11+2151C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951664 | ||||||
chr16:89951682
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0108 | 12 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+2169T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951682 | ||||||
chr16:89951778
|
T | C | 14 | a0001c0001t0001g0155a0001c0001t0001g0176a0001c0001t0002g0003others(11): Show | 33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11+2265T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951778 | ||||||
chr16:89951782
|
G | C | 1 | a0001c0001t0002g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-11+2269G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951782 | ||||||
chr16:89951827
|
C | CACACACA others(17): Show |
2 | a0001c0002t0017g0082a0001c0002t0017g0083 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+2324_-11+2347d others(26): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89951827 | |||||
chr16:89951874
|
A | G | 1 | a0001c0001t0023g0053 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-11+2361A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951874 | ||||||
chr16:89951879
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-10-2364A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951879 | ||||||
chr16:89951880
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-10-2363G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951880 | ||||||
chr16:89951881
|
A | T | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-10-2362A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951881 | ||||||
chr16:89951881
|
AT | A | 37 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0085others(34): Show | 48 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10-2348delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 89951881 | |||||
chr16:89951981
|
T | C | 39 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0029others(36): Show | 51 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-2262T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89951981 | ||||||
chr16:89952014
|
G | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0085others(33): Show | 47 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.-10-2229G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952014 | ||||||
chr16:89952035
|
A | G | 35 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0085others(32): Show | 46 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-10-2208A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952035 | ||||||
chr16:89952065
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-10-2178G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952065 | ||||||
chr16:89952068
|
A | G | 40 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0085others(37): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10-2175A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952068 | ||||||
chr16:89952077
|
A | C | 7 | a0001c0001t0016g0182a0002c0004t0001g0013a0002c0004t0001g0220others(4): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-2166A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952077 | ||||||
chr16:89952078
|
T | C | 7 | a0001c0001t0016g0182a0002c0004t0001g0013a0002c0004t0001g0220others(4): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-2165T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952078 | ||||||
chr16:89952086
|
C | T | 7 | a0001c0002t0006g0073a0002c0004t0001g0013a0002c0004t0001g0220others(4): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-2157C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952086 | ||||||
chr16:89952088
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-10-2155A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952088 | ||||||
chr16:89952096
|
T | C | 105 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0023others(102): Show | 149 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-10-2147T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952096 | ||||||
chr16:89952217
|
A | C | 37 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0085others(34): Show | 48 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10-2026A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952217 | ||||||
chr16:89952228
|
C | T | 6 | a0002c0004t0001g0013a0002c0004t0001g0220a0002c0004t0001g0221others(3): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-2015C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952228 | ||||||
chr16:89952449
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-10-1794C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952449 | ||||||
chr16:89952580
|
G | C | 22 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0074others(19): Show | 27 | HG00639.hp1 HG01192.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10-1663G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952580 | ||||||
chr16:89952653
|
C | T | 6 | a0001c0001t0001g0115a0001c0002t0005g0014a0001c0002t0005g0054others(3): Show | 8 | HG02602.hp1 HG02738.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-1590C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952653 | ||||||
chr16:89952676
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-10-1567T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952676 | ||||||
chr16:89952786
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-1457C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952786 | ||||||
chr16:89952818
|
C | T | 1 | a0001c0002t0006g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10-1425C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952818 | ||||||
chr16:89952857
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-10-1386A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952857 | ||||||
chr16:89952990
|
C | T | 31 | a0001c0001t0001g0115a0001c0001t0003g0015a0001c0001t0003g0025others(28): Show | 40 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-10-1253C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89952990 | ||||||
chr16:89953236
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-10-1007C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953236 | ||||||
chr16:89953254
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-10-989C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953254 | ||||||
chr16:89953271
|
C | T | 2 | a0001c0002t0017g0082a0001c0002t0017g0083 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-972C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953271 | ||||||
chr16:89953275
|
T | C | 3 | a0001c0001t0004g0009a0001c0001t0004g0062a0001c0001t0004g0063 | 6 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-968T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953275 | ||||||
chr16:89953825
|
T | C | 5 | a0001c0002t0007g0088a0001c0002t0007g0114a0001c0002t0011g0078others(2): Show | 5 | HG00099.hp2 HG01109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-418T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953825 | ||||||
chr16:89953933
|
T | C | 64 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0026others(61): Show | 98 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-10-310T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953933 | ||||||
chr16:89953938
|
A | C | 68 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0026others(65): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-10-305A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953938 | ||||||
chr16:89953948
|
T | C | 1 | a0001c0001t0001g0032 | 2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-10-295T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953948 | ||||||
chr16:89953958
|
G | T | 1 | a0001c0001t0002g0181 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-10-285G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953958 | ||||||
chr16:89953998
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-10-245G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 2/12 | chr16 | 89953998 | ||||||
chr16:89954389
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.124+13G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954389 | ||||||
chr16:89954392
|
A | C | 2 | a0001c0002t0011g0213a0001c0002t0024g0212 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.124+16A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954392 | ||||||
chr16:89954453
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(170): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.124+77C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954453 | ||||||
chr16:89954656
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.124+280C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954656 | ||||||
chr16:89954701
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0074others(8): Show | 14 | HG01192.hp1 HG02615.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.124+325G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954701 | ||||||
chr16:89954730
|
T | A | 1 | a0001c0001t0001g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.124+354T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954730 | ||||||
chr16:89954886
|
A | G | 16 | a0001c0001t0001g0163a0001c0001t0001g0180a0001c0001t0003g0075others(13): Show | 17 | HG01243.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-283A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89954886 | ||||||
chr16:89955059
|
T | G | 3 | a0001c0001t0004g0009a0001c0001t0004g0062a0001c0001t0004g0063 | 6 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-110T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955059 | ||||||
chr16:89955111
|
G | C | 2 | a0001c0002t0012g0065a0001c0002t0012g0070 | 2 | HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.125-58G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955111 | ||||||
chr16:89955140
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.125-29G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955140 | ||||||
chr16:89955157
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-12G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955157 | ||||||
chr16:89955161
|
T | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0155others(16): Show | 42 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.125-8T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 3/12 | chr16 | 89955161 | ||||||
chr16:89955277
|
A | G | 21 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0002g0003others(18): Show | 41 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.222+11A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955277 | ||||||
chr16:89955303
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.222+37G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955303 | ||||||
chr16:89955355
|
G | T | 1 | a0001c0008t0005g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.222+89G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955355 | ||||||
chr16:89955452
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.222+186C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955452 | ||||||
chr16:89955485
|
C | T | 2 | a0001c0002t0011g0213a0001c0002t0024g0212 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.222+219C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955485 | ||||||
chr16:89955517
|
T | C | 2 | a0001c0002t0011g0213a0001c0002t0024g0212 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.222+251T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955517 | ||||||
chr16:89955629
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+363G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955629 | ||||||
chr16:89955663
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.222+397T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955663 | ||||||
chr16:89955715
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.222+449C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955715 | ||||||
chr16:89955729
|
T | C | 14 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(11): Show | 33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+463T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955729 | ||||||
chr16:89955778
|
T | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0201 | 2 | HG01192.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.222+512T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955778 | ||||||
chr16:89955779
|
A | T | 2 | a0001c0001t0019g0177a0002c0005t0009g0223 | 2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.222+513A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955779 | ||||||
chr16:89955795
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.222+529G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955795 | ||||||
chr16:89955799
|
G | A | 7 | a0001c0001t0001g0217a0001c0002t0007g0048a0001c0002t0007g0209others(4): Show | 8 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+533G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955799 | ||||||
chr16:89955825
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+559C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955825 | ||||||
chr16:89955828
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.222+562T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955828 | ||||||
chr16:89955838
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+572T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955838 | ||||||
chr16:89955839
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+573G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955839 | ||||||
chr16:89955848
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.222+582G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955848 | ||||||
chr16:89955861
|
A | G | 14 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(11): Show | 33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+595A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955861 | ||||||
chr16:89955888
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0010g0027a0001c0001t0010g0079others(1): Show | 5 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+622C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89955888 | ||||||
chr16:89956076
|
G | GA | 51 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0176others(48): Show | 77 | HG00099.hp2 HG00438.hp2 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.222+819dupA | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 89956076 | |||||
chr16:89956094
|
A | G | 1 | a0001c0008t0005g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.222+828A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956094 | ||||||
chr16:89956116
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.222+850A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956116 | ||||||
chr16:89956195
|
C | T | 13 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(10): Show | 32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.222+929C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956195 | ||||||
chr16:89956228
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222+962G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956228 | ||||||
chr16:89956283
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.222+1017C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956283 | ||||||
chr16:89956285
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.222+1019T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956285 | ||||||
chr16:89956330
|
C | T | 13 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(10): Show | 32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.222+1064C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956330 | ||||||
chr16:89956374
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.222+1108C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956374 | ||||||
chr16:89956375
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0102a0001c0001t0001g0149others(1): Show | 5 | HG00733.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+1109G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956375 | ||||||
chr16:89956489
|
T | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(160): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.223-1022T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956489 | ||||||
chr16:89956534
|
C | T | 6 | a0001c0001t0001g0217a0001c0002t0007g0048a0001c0002t0007g0209others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-977C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956534 | ||||||
chr16:89956544
|
C | T | 1 | a0001c0001t0019g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.223-967C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956544 | ||||||
chr16:89956566
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0140 | 3 | HG03927.hp2 NA18977.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.223-945C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956566 | ||||||
chr16:89956679
|
A | AT | 43 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0138others(40): Show | 52 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.223-822dupT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 89956679 | |||||
chr16:89956766
|
C | A | 1 | a0001c0009t0022g0210 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.223-745C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956766 | ||||||
chr16:89956864
|
A | G | 15 | a0001c0001t0001g0122a0001c0001t0003g0015a0001c0001t0003g0025others(12): Show | 22 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.223-647A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956864 | ||||||
chr16:89956959
|
C | G | 1 | a0001c0009t0022g0210 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.223-552C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956959 | ||||||
chr16:89956961
|
C | G | 5 | a0001c0002t0011g0078a0001c0002t0011g0213a0001c0002t0017g0082others(2): Show | 5 | HG00099.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-550C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956961 | ||||||
chr16:89956997
|
C | A | 19 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(16): Show | 41 | HG00438.hp2 HG00639.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.223-514C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89956997 | ||||||
chr16:89957031
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.223-480C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957031 | ||||||
chr16:89957061
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.223-450G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957061 | ||||||
chr16:89957112
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.223-399C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957112 | ||||||
chr16:89957236
|
AAGGAAGT others(26): Show |
A | 1 | a0004c0007t0005g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.223-273_223-241del others(33): Show |
DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 89957236 | |||||
chr16:89957284
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.223-227G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957284 | ||||||
chr16:89957417
|
C | T | 2 | a0001c0002t0014g0206a0001c0002t0014g0207 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.223-94C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957417 | ||||||
chr16:89957440
|
C | T | 1 | a0001c0001t0001g0034 | 2 | NA18970.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.223-71C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957440 | ||||||
chr16:89957493
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(51): Show | 114 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.223-18C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 4/12 | chr16 | 89957493 | ||||||
chr16:89957683
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.372+23G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957683 | ||||||
chr16:89957778
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.372+118A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957778 | ||||||
chr16:89957794
|
G | A | 40 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0176others(37): Show | 60 | HG00099.hp2 HG00438.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.372+134G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957794 | ||||||
chr16:89957798
|
A | G | 62 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0176others(59): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.372+138A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957798 | ||||||
chr16:89957820
|
C | T | 13 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(10): Show | 32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.372+160C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89957820 | ||||||
chr16:89958005
|
C | T | 12 | a0001c0001t0003g0015a0001c0001t0003g0050a0001c0001t0003g0057others(9): Show | 18 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+345C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958005 | ||||||
chr16:89958025
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.372+365G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958025 | ||||||
chr16:89958039
|
T | C | 13 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(10): Show | 32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.372+379T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958039 | ||||||
chr16:89958248
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.372+588C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958248 | ||||||
chr16:89958255
|
T | G | 7 | a0001c0001t0001g0217a0001c0002t0007g0048a0001c0002t0007g0209others(4): Show | 8 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+595T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958255 | ||||||
chr16:89958306
|
C | G | 12 | a0001c0002t0011g0078a0001c0002t0011g0213a0001c0002t0017g0082others(9): Show | 12 | HG00099.hp2 HG01081.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+646C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958306 | ||||||
chr16:89958317
|
G | A | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.372+657G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958317 | ||||||
chr16:89958439
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.373-575G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958439 | ||||||
chr16:89958458
|
C | T | 13 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(10): Show | 32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.373-556C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958458 | ||||||
chr16:89958491
|
T | A | 20 | a0001c0001t0001g0176a0001c0001t0001g0217a0001c0001t0002g0003others(17): Show | 40 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.373-523T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958491 | ||||||
chr16:89958492
|
A | G | 20 | a0001c0001t0001g0176a0001c0001t0001g0217a0001c0001t0002g0003others(17): Show | 40 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.373-522A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958492 | ||||||
chr16:89958506
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.373-508A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958506 | ||||||
chr16:89958558
|
A | C | 1 | a0001c0001t0019g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.373-456A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958558 | ||||||
chr16:89958562
|
C | G | 25 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0002t0006g0051others(22): Show | 26 | HG00099.hp2 HG01081.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.373-452C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958562 | ||||||
chr16:89958713
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.373-301G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958713 | ||||||
chr16:89958717
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.373-297G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958717 | ||||||
chr16:89958727
|
C | T | 14 | a0001c0001t0001g0176a0001c0001t0001g0201a0001c0001t0002g0003others(11): Show | 33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.373-287C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958727 | ||||||
chr16:89958881
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.373-133A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958881 | ||||||
chr16:89958912
|
C | T | 29 | a0001c0001t0001g0176a0001c0001t0001g0217a0001c0001t0002g0003others(26): Show | 52 | HG00438.hp2 HG00639.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.373-102C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 5/12 | chr16 | 89958912 | ||||||
chr16:89959213
|
G | A | 1 | a0001c0001t0010g0027 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.514+58G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959213 | ||||||
chr16:89959232
|
G | C | 27 | a0001c0001t0001g0176a0001c0001t0001g0217a0001c0001t0002g0003others(24): Show | 50 | HG00438.hp2 HG00639.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.514+77G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959232 | ||||||
chr16:89959411
|
G | T | 3 | a0001c0003t0008g0178a0001c0003t0008g0211a0001c0003t0008g0224 | 3 | HG01081.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.514+256G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959411 | ||||||
chr16:89959524
|
T | G | 1 | a0001c0001t0019g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.514+369T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959524 | ||||||
chr16:89959531
|
A | G | 1 | a0001c0001t0001g0043 | 2 | NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.514+376A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959531 | ||||||
chr16:89959533
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.514+378C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959533 | ||||||
chr16:89959544
|
G | T | 1 | a0001c0001t0003g0025 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.514+389G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959544 | ||||||
chr16:89959597
|
C | A | 14 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(11): Show | 33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.514+442C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959597 | ||||||
chr16:89959641
|
C | G | 14 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(11): Show | 33 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.514+486C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959641 | ||||||
chr16:89959662
|
T | A | 7 | a0001c0002t0005g0014a0001c0002t0005g0046a0001c0002t0005g0054others(4): Show | 10 | HG00639.hp1 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+507T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959662 | ||||||
chr16:89959688
|
G | A | 8 | a0001c0001t0001g0217a0001c0002t0007g0048a0001c0002t0007g0209others(5): Show | 9 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+533G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959688 | ||||||
chr16:89959698
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.514+543C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959698 | ||||||
chr16:89959744
|
A | G | 71 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0176others(68): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.514+589A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959744 | ||||||
chr16:89959760
|
G | C | 7 | a0001c0002t0005g0014a0001c0002t0005g0046a0001c0002t0005g0054others(4): Show | 10 | HG00639.hp1 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+605G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959760 | ||||||
chr16:89959796
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.514+641C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959796 | ||||||
chr16:89959804
|
C | T | 1 | a0002c0004t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.514+649C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959804 | ||||||
chr16:89959934
|
G | A | 2 | a0001c0002t0017g0082a0001c0002t0017g0083 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.514+779G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959934 | ||||||
chr16:89959946
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.514+791G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959946 | ||||||
chr16:89959964
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0074others(11): Show | 20 | HG01192.hp1 HG02257.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.514+809C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89959964 | ||||||
chr16:89960006
|
G | A | 1 | a0001c0002t0011g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.514+851G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960006 | ||||||
chr16:89960080
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.515-851G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960080 | ||||||
chr16:89960081
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.515-850C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960081 | ||||||
chr16:89960104
|
T | C | 68 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0176others(65): Show | 97 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.515-827T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960104 | ||||||
chr16:89960349
|
T | G | 1 | a0001c0001t0023g0053 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.515-582T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960349 | ||||||
chr16:89960367
|
A | G | 13 | a0001c0001t0001g0176a0001c0001t0002g0003a0001c0001t0002g0012others(10): Show | 32 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.515-564A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960367 | ||||||
chr16:89960502
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0102a0001c0001t0001g0126others(2): Show | 6 | HG00733.hp1 HG01346.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-429C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960502 | ||||||
chr16:89960571
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(56): Show | 122 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.515-360T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960571 | ||||||
chr16:89960600
|
C | T | 1 | a0001c0001t0023g0053 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.515-331C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960600 | ||||||
chr16:89960638
|
G | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0087 | 2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.515-293G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960638 | ||||||
chr16:89960792
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0102a0001c0001t0001g0126others(2): Show | 6 | HG00733.hp1 HG01346.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-139C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960792 | ||||||
chr16:89960861
|
C | T | 4 | a0001c0001t0001g0180a0002c0005t0009g0022a0002c0005t0009g0096others(1): Show | 6 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-70C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 6/12 | chr16 | 89960861 | ||||||
chr16:89961218
|
A | T | 72 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0176others(69): Show | 103 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.679+123A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961218 | ||||||
chr16:89961274
|
G | A | 1 | a0001c0001t0021g0107 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.679+179G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961274 | ||||||
chr16:89961297
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0104 | 4 | HG01891.hp1 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+202C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961297 | ||||||
chr16:89961398
|
C | T | 1 | a0001c0001t0001g0011 | 4 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+303C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961398 | ||||||
chr16:89961414
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0074others(11): Show | 21 | HG00639.hp1 HG01192.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.679+319A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961414 | ||||||
chr16:89961430
|
G | A | 35 | a0001c0001t0001g0026a0001c0001t0003g0015a0001c0001t0003g0025others(32): Show | 40 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.680-307G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961430 | ||||||
chr16:89961476
|
C | G | 6 | a0001c0002t0005g0014a0001c0002t0005g0054a0001c0002t0005g0060others(3): Show | 8 | HG01884.hp1 HG02602.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-261C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961476 | ||||||
chr16:89961536
|
G | T | 31 | a0001c0001t0001g0026a0001c0001t0001g0180a0001c0001t0003g0015others(28): Show | 38 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.680-201G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961536 | ||||||
chr16:89961640
|
C | T | 1 | a0001c0001t0019g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.680-97C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961640 | ||||||
chr16:89961645
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.680-92G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961645 | ||||||
chr16:89961674
|
G | A | 2 | a0001c0002t0011g0213a0001c0002t0024g0212 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.680-63G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961674 | ||||||
chr16:89961698
|
T | G | 44 | a0001c0001t0001g0026a0001c0001t0001g0180a0001c0001t0003g0015others(41): Show | 52 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.680-39T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961698 | ||||||
chr16:89961715
|
C | T | 3 | a0001c0001t0010g0027a0001c0001t0010g0079a0001c0001t0010g0080 | 4 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-22C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 7/12 | chr16 | 89961715 | ||||||
chr16:89961996
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0137a0001c0001t0001g0139 | 3 | HG02738.hp1 HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.808-16C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 8/12 | chr16 | 89961996 | ||||||
chr16:89962181
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.921+56G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962181 | ||||||
chr16:89962268
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.921+143C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962268 | ||||||
chr16:89962363
|
T | C | 10 | a0001c0001t0001g0085a0001c0002t0011g0078a0001c0002t0011g0213others(7): Show | 10 | HG00099.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.921+238T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962363 | ||||||
chr16:89962387
|
C | T | 6 | a0001c0002t0005g0014a0001c0002t0005g0054a0001c0002t0005g0060others(3): Show | 8 | HG01884.hp1 HG02602.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+262C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962387 | ||||||
chr16:89962581
|
G | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0160 | 3 | NA18945.hp2 NA19064.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.921+456G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962581 | ||||||
chr16:89962697
|
G | C | 12 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0093others(9): Show | 31 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.921+572G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962697 | ||||||
chr16:89962841
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.922-522G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962841 | ||||||
chr16:89962994
|
G | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0102others(11): Show | 18 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.922-369G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962994 | ||||||
chr16:89962997
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.922-366C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89962997 | ||||||
chr16:89963009
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 77 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.922-354G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963009 | ||||||
chr16:89963030
|
G | A | 1 | a0001c0002t0005g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.922-333G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963030 | ||||||
chr16:89963089
|
G | A | 1 | a0001c0001t0001g0032 | 2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.922-274G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963089 | ||||||
chr16:89963157
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.922-206G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963157 | ||||||
chr16:89963172
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.922-191C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963172 | ||||||
chr16:89963252
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0173a0001c0001t0013g0038others(1): Show | 6 | HG00099.hp1 HG01074.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.922-111C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963252 | ||||||
chr16:89963305
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.922-58A>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963305 | ||||||
chr16:89963342
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.922-21C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 9/12 | chr16 | 89963342 | ||||||
chr16:89963460
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1002+17G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963460 | ||||||
chr16:89963491
|
T | C | 7 | a0001c0002t0007g0048a0001c0002t0007g0088a0001c0002t0007g0114others(4): Show | 8 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002+48T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963491 | ||||||
chr16:89963521
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0172 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1002+78C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963521 | ||||||
chr16:89963522
|
G | A | 17 | a0001c0001t0001g0180a0001c0002t0007g0048a0001c0002t0007g0088others(14): Show | 20 | HG01081.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1002+79G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963522 | ||||||
chr16:89963640
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002+197C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963640 | ||||||
chr16:89963655
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1002+212T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963655 | ||||||
chr16:89963810
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1003-360C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963810 | ||||||
chr16:89963878
|
G | C | 3 | a0001c0001t0010g0027a0001c0001t0010g0079a0001c0001t0010g0080 | 4 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-292G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963878 | ||||||
chr16:89963947
|
T | C | 93 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0026others(90): Show | 131 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1003-223T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89963947 | ||||||
chr16:89964012
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1003-158G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89964012 | ||||||
chr16:89964066
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1003-104G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89964066 | ||||||
chr16:89964122
|
G | C | 11 | a0001c0002t0014g0206a0001c0002t0014g0207a0001c0003t0008g0076others(8): Show | 13 | HG01081.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1003-48G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 10/12 | chr16 | 89964122 | ||||||
chr16:89964362
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(54): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1143+52A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964362 | ||||||
chr16:89964365
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1143+55G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964365 | ||||||
chr16:89964409
|
G | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0137a0001c0001t0001g0139 | 3 | HG02738.hp1 HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1144-57G>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964409 | ||||||
chr16:89964449
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1144-17C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 11/12 | chr16 | 89964449 | ||||||
chr16:89964595
|
C | T | 1 | a0001c0001t0002g0190 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1253+20C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964595 | ||||||
chr16:89964738
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1253+163T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964738 | ||||||
chr16:89964814
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0144 | 2 | NA18939.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1253+239C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964814 | ||||||
chr16:89964819
|
C | A | 1 | a0001c0001t0002g0183 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1253+244C>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964819 | ||||||
chr16:89964848
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1253+273C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964848 | ||||||
chr16:89964954
|
T | G | 3 | a0002c0005t0009g0022a0002c0005t0009g0096a0002c0005t0009g0223 | 5 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253+379T>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964954 | ||||||
chr16:89964964
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0197a0003c0006t0001g0020 | 4 | NA18951.hp1 NA18968.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+389G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964964 | ||||||
chr16:89964986
|
AT | A | 9 | a0001c0002t0007g0048a0001c0002t0007g0088a0001c0002t0007g0114others(6): Show | 10 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1253+417delT | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr16 | 89964986 | |||||
chr16:89964994
|
A | C | 9 | a0001c0002t0007g0048a0001c0002t0007g0088a0001c0002t0007g0114others(6): Show | 10 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1253+419A>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89964994 | ||||||
chr16:89965011
|
G | A | 12 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0093others(9): Show | 31 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.1253+436G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965011 | ||||||
chr16:89965019
|
T | A | 12 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0093others(9): Show | 31 | HG00438.hp2 HG01175.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.1253+444T>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965019 | ||||||
chr16:89965072
|
C | T | 1 | a0001c0001t0003g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1253+497C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965072 | ||||||
chr16:89965320
|
T | C | 1 | a0001c0009t0022g0210 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1254-541T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965320 | ||||||
chr16:89965357
|
A | G | 1 | a0001c0002t0006g0225 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1254-504A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965357 | ||||||
chr16:89965408
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1254-453A>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965408 | ||||||
chr16:89965640
|
T | C | 52 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0085others(49): Show | 63 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1254-221T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965640 | ||||||
chr16:89965687
|
C | T | 1 | a0001c0002t0025g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1254-174C>T | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965687 | ||||||
chr16:89965709
|
G | A | 1 | a0001c0002t0024g0212 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1254-152G>A | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965709 | ||||||
chr16:89965741
|
T | C | 50 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0131others(47): Show | 58 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1254-120T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965741 | ||||||
chr16:89965758
|
G | C | 1 | a0001c0001t0001g0026 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1254-103G>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965758 | ||||||
chr16:89965824
|
T | C | 39 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0002t0005g0014others(36): Show | 45 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1254-37T>C | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965824 | ||||||
chr16:89965847
|
C | G | 46 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0002t0005g0014others(43): Show | 52 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1254-14C>G | DEF8 | ENSG00000140995.17 | transcript | ENST00000563594.6 | protein_coding | 12/12 | chr16 | 89965847 |