geneid | 79269 |
---|---|
ensemblid | ENSG00000122741.16 |
hgncid | 23686 |
symbol | DCAF10 |
name | DDB1 and CUL4 associated factor 10 |
refseq_nuc | NM_024345.5 |
refseq_prot | NP_077321.3 |
ensembl_nuc | ENST00000377724.8 |
ensembl_prot | ENSP00000366953.3 |
mane_status | MANE Select |
chr | chr9 |
start | 37800797 |
end | 37867664 |
strand | + |
ver | v1.2 |
region | chr9:37800797-37867664 |
region5000 | chr9:37795797-37872664 |
regionname0 | DCAF10_chr9_37800797_37867664 |
regionname5000 | DCAF10_chr9_37795797_37872664 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 559 | 354 | 77 | 72 | 147 | 12 | 44 | 111 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0002 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0003 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1680 | 348 | 73 | 71 | 146 | 12 | 44 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
c0002 | 0/0 | 1680 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
c0003 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
c0004 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
c0005 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
c0006 | 0/0 | 1680 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
c0007 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 6227 | 108 | 19 | 24 | 50 | 3 | 10 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0002 | 0/0 | 6226 | 51 | 5 | 9 | 25 | 2 | 10 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0003 | 0/0 | 6227 | 40 | 2 | 13 | 16 | 1 | 8 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0004 | 0/0 | 6227 | 27 | 10 | 4 | 7 | 2 | 4 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0005 | 0/0 | 6242 | 11 | 1 | 2 | 6 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0006 | 0/0 | 6227 | 9 | 1 | 3 | 4 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0007 | 0/0 | 6226 | 8 | 1 | 0 | 7 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0008 | 0/0 | 6225 | 7 | 7 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0009 | 0/0 | 6243 | 6 | 0 | 0 | 5 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0010 | 0/0 | 6228 | 5 | 1 | 0 | 3 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0011 | 0/0 | 6227 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0012 | 0/0 | 6228 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0013 | 0/0 | 6227 | 4 | 0 | 4 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0014 | 0/0 | 6222 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0015 | 0/0 | 6230 | 4 | 3 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0016 | 0/0 | 6227 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0017 | 0/0 | 6226 | 3 | 0 | 0 | 2 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0018 | 0/0 | 6225 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0019 | 0/0 | 6232 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0020 | 0/0 | 6232 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0021 | 0/0 | 6232 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0022 | 0/0 | 6227 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0023 | 0/0 | 6228 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0024 | 0/0 | 6227 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0025 | 0/0 | 6227 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0026 | 0/0 | 6227 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0027 | 0/0 | 6244 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0028 | 0/0 | 6242 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0029 | 0/0 | 6227 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0030 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0031 | 0/0 | 6231 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0032 | 0/0 | 6232 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0033 | 0/0 | 6228 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0034 | 0/0 | 6226 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0035 | 0/0 | 6228 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0036 | 0/0 | 6228 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0037 | 0/0 | 6228 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0038 | 0/0 | 6228 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0039 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0040 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0041 | 0/0 | 6227 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0042 | 0/0 | 6228 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0043 | 0/0 | 6227 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0044 | 0/0 | 6227 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0045 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0046 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0047 | 0/0 | 6226 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0048 | 0/0 | 6228 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0049 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0050 | 0/0 | 6226 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0051 | 0/0 | 6226 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0052 | 0/0 | 6226 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0053 | 0/0 | 6226 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0054 | 0/0 | 6226 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0055 | 0/0 | 6226 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0056 | 0/0 | 6226 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0057 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0058 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0059 | 0/0 | 6245 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0060 | 0/0 | 6243 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0061 | 0/0 | 6243 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0062 | 0/0 | 6234 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
t0063 | 0/0 | 6230 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1680 | 348 | 73 | 71 | 146 | 12 | 44 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0002 | 0/0 | 1680 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0003 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0004 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0006 | 0/0 | 1680 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0002c0005 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0003c0007 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7906 | 107 | 19 | 24 | 49 | 3 | 10 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0002 | 0/0 | 7905 | 51 | 5 | 9 | 25 | 2 | 10 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0003 | 0/0 | 7906 | 39 | 2 | 12 | 16 | 1 | 8 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0004 | 0/0 | 7906 | 24 | 7 | 4 | 7 | 2 | 4 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0005 | 0/0 | 7921 | 11 | 1 | 2 | 6 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0006 | 0/0 | 7906 | 9 | 1 | 3 | 4 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0007 | 0/0 | 7905 | 8 | 1 | 0 | 7 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0008 | 0/0 | 7904 | 6 | 6 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0009 | 0/0 | 7922 | 6 | 0 | 0 | 5 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0010 | 0/0 | 7907 | 5 | 1 | 0 | 3 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0011 | 0/0 | 7906 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0012 | 0/0 | 7907 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0013 | 0/0 | 7906 | 4 | 0 | 4 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0014 | 0/0 | 7901 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0015 | 0/0 | 7909 | 4 | 3 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0016 | 0/0 | 7906 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0017 | 0/0 | 7905 | 3 | 0 | 0 | 2 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0018 | 0/0 | 7904 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0019 | 0/0 | 7911 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0020 | 0/0 | 7911 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0021 | 0/0 | 7911 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0022 | 0/0 | 7906 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0023 | 0/0 | 7907 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0024 | 0/0 | 7906 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0025 | 0/0 | 7906 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0026 | 0/0 | 7906 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0027 | 0/0 | 7923 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0028 | 0/0 | 7921 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0029 | 0/0 | 7906 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0031 | 0/0 | 7910 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0032 | 0/0 | 7911 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0033 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0034 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0035 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0036 | 0/0 | 7907 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0037 | 0/0 | 7907 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0038 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0039 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0040 | 0/0 | 7906 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0041 | 0/0 | 7906 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0042 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0043 | 0/0 | 7906 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0044 | 0/0 | 7906 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0045 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0046 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0048 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0049 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0050 | 0/0 | 7905 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0051 | 0/0 | 7905 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0052 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0053 | 0/0 | 7905 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0054 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0055 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0056 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0057 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0058 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0059 | 0/0 | 7924 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0060 | 0/0 | 7922 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0061 | 0/0 | 7922 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0062 | 0/0 | 7913 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0001t0063 | 0/0 | 7909 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0002t0004 | 0/0 | 7906 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0003t0030 | 0/0 | 7924 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0004t0047 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0001c0006t0003 | 0/0 | 7906 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0002c0005t0001 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
a0003c0007t0008 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | copy fasta | chr9 | 37795797 | 37872664 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0012g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0013g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0015g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0016g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0016g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0016g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0017g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0017g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0017g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0018g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0018g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0021g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0022g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0022g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0023g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0023g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0024g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0024g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0025g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0025g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0026g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0027g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0027g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0028g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0028g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0029g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0031g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0032g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0033g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0034g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0035g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0036g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0037g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0038g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0039g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0040g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0041g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0042g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0043g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0044g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0045g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0046g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0048g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0049g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0050g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0051g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0052g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0053g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0054g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0055g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0056g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0057g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0058g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0059g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0060g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0061g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0062g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0001t0063g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0003t0030g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0004t0047g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0001c0006t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0002c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
a0003c0007t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0084 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00140 | hp1 | a0001 | c0001 | t0024 | g0215 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0003 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0175 | EUR | FIN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00438 | hp1 | a0001 | c0001 | t0035 | g0154 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00438 | hp2 | a0001 | c0001 | t0010 | g0229 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00597 | hp1 | a0001 | c0001 | t0058 | g0097 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00639 | hp1 | a0001 | c0006 | t0003 | g0186 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00639 | hp2 | a0001 | c0001 | t0026 | g0006 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00733 | hp2 | a0001 | c0001 | t0013 | g0056 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00735 | hp1 | a0001 | c0001 | t0041 | g0228 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00738 | hp2 | a0001 | c0001 | t0026 | g0006 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00741 | hp1 | a0001 | c0001 | t0016 | g0160 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01081 | hp1 | a0001 | c0001 | t0028 | g0028 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01106 | hp2 | a0001 | c0001 | t0016 | g0159 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01109 | hp2 | a0001 | c0001 | t0023 | g0177 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01192 | hp2 | a0001 | c0001 | t0028 | g0027 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01243 | hp1 | a0001 | c0001 | t0021 | g0001 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01256 | hp1 | a0001 | c0001 | t0013 | g0059 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0057 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0151 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01361 | hp1 | a0001 | c0001 | t0037 | g0187 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0253 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01496 | hp2 | a0001 | c0001 | t0063 | g0039 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0025 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01515 | hp2 | a0001 | c0001 | t0016 | g0176 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0309 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01975 | hp1 | a0001 | c0001 | t0043 | g0157 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0322 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0085 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02074 | hp1 | a0001 | c0004 | t0047 | g0287 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02080 | hp2 | a0001 | c0001 | t0057 | g0073 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0288 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02155 | hp1 | a0001 | c0001 | t0045 | g0262 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02165 | hp1 | a0001 | c0001 | t0034 | g0339 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02257 | hp2 | a0001 | c0001 | t0031 | g0347 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02280 | hp1 | a0001 | c0002 | t0004 | g0179 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02572 | hp2 | a0001 | c0001 | t0038 | g0340 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02622 | hp2 | a0001 | c0001 | t0062 | g0012 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02630 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02717 | hp1 | a0001 | c0003 | t0030 | g0040 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02717 | hp2 | a0001 | c0001 | t0025 | g0170 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02738 | hp1 | a0001 | c0001 | t0024 | g0216 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02818 | hp1 | a0001 | c0001 | t0032 | g0050 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02922 | hp2 | a0001 | c0001 | t0021 | g0001 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02965 | hp1 | a0001 | c0001 | t0051 | g0141 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02965 | hp2 | a0001 | c0001 | t0053 | g0240 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02970 | hp1 | a0001 | c0001 | t0022 | g0345 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02976 | hp2 | a0001 | c0001 | t0018 | g0341 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03017 | hp1 | a0001 | c0001 | t0044 | g0231 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03041 | hp1 | a0001 | c0001 | t0022 | g0346 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03139 | hp1 | a0001 | c0001 | t0020 | g0049 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0293 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03209 | hp1 | a0001 | c0001 | t0015 | g0032 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0088 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03486 | hp1 | a0001 | c0001 | t0012 | g0055 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03486 | hp2 | a0001 | c0001 | t0025 | g0173 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03491 | hp2 | a0001 | c0001 | t0050 | g0217 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03516 | hp1 | a0001 | c0001 | t0020 | g0048 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03540 | hp2 | a0001 | c0001 | t0014 | g0202 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0026 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03688 | hp1 | a0001 | c0001 | t0036 | g0226 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0257 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03710 | hp2 | a0001 | c0001 | t0010 | g0108 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03831 | hp1 | a0001 | c0001 | t0061 | g0030 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0209 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04115 | hp2 | a0001 | c0001 | t0017 | g0076 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04184 | hp1 | a0001 | c0001 | t0023 | g0089 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04184 | hp2 | a0001 | c0001 | t0059 | g0034 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04199 | hp1 | a0001 | c0001 | t0009 | g0022 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0274 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0334 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18906 | hp2 | a0003 | c0007 | t0008 | g0047 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18943 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18946 | hp1 | a0001 | c0001 | t0054 | g0007 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18948 | hp2 | a0001 | c0001 | t0015 | g0035 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0265 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18957 | hp1 | a0001 | c0001 | t0027 | g0014 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18957 | hp2 | a0002 | c0005 | t0001 | g0070 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18959 | hp2 | a0001 | c0001 | t0052 | g0133 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18960 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18965 | hp2 | a0001 | c0001 | t0049 | g0119 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18967 | hp2 | a0001 | c0001 | t0039 | g0279 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18970 | hp2 | a0001 | c0001 | t0042 | g0276 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18974 | hp2 | a0001 | c0001 | t0048 | g0237 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18977 | hp2 | a0001 | c0001 | t0056 | g0307 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18978 | hp1 | a0001 | c0001 | t0055 | g0264 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18979 | hp1 | a0001 | c0001 | t0011 | g0238 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18979 | hp2 | a0001 | c0001 | t0007 | g0268 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18980 | hp2 | a0001 | c0001 | t0046 | g0100 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18988 | hp1 | a0001 | c0001 | t0027 | g0015 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18989 | hp1 | a0001 | c0001 | t0011 | g0233 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18995 | hp1 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18995 | hp2 | a0001 | c0001 | t0006 | g0259 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19000 | hp1 | a0001 | c0001 | t0011 | g0230 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0316 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19011 | hp1 | a0001 | c0001 | t0011 | g0232 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0129 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19056 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19057 | hp1 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19060 | hp1 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0271 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19076 | hp1 | a0001 | c0001 | t0009 | g0037 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19079 | hp1 | a0001 | c0001 | t0007 | g0292 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0245 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19091 | hp2 | a0001 | c0001 | t0017 | g0328 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19240 | hp1 | a0001 | c0001 | t0014 | g0201 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA19240 | hp2 | a0001 | c0001 | t0033 | g0053 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0019 | AFR | ASW | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0178 | AFR | ASW | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20752 | hp1 | a0001 | c0001 | t0029 | g0211 | EUR | TSI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | GIH | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0343 | SAS | GIH | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG01123 | hp2 | a0001 | c0001 | t0060 | g0011 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0184 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0051 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02559 | hp1 | a0001 | c0001 | t0019 | g0052 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG06807 | hp1 | a0001 | c0001 | t0040 | g0199 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18955 | hp1 | a0001 | c0001 | t0011 | g0234 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA18955 | hp2 | a0001 | c0001 | t0017 | g0327 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0342 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0213 | REF | REF | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0329 | REF | REF | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:37800873
|
C | T | 1 | a0003 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.7C>T | p.Pro3Ser | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 77/7906 | 7/1680 | 3/559 | chr9 | 37800873 | ||
chr9:37860086
|
G | A | 1 | a0002 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.1204G>A | p.Glu402Lys | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/7 | 1274/7906 | 1204/1680 | 402/559 | chr9 | 37860086 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:37800908
|
G | A | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.42G>A | p.Ser14Ser | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 112/7906 | 42/1680 | 14/559 | chr9 | 37800908 | ||
chr9:37800965
|
G | A | 1 | a0001c0004 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.99G>A | p.Gly33Gly | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 169/7906 | 99/1680 | 33/559 | chr9 | 37800965 | ||
chr9:37801370
|
C | T | 1 | a0001c0006 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.504C>T | p.His168His | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 574/7906 | 504/1680 | 168/559 | chr9 | 37801370 | ||
chr9:37861481
|
G | A | 1 | a0001c0002 | 3 | HG02280.hp1 HG02486.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.1653G>A | p.Arg551Arg | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1723/7906 | 1653/1680 | 551/559 | chr9 | 37861481 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:37800841
|
C | A | 1 | a0001c0001t0029 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 26 | chr9 | 37800841 | |||||
chr9:37861684
|
A | ATC | 10 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(7): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*179_*180dupTC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 181 | INFO_REALIGN_3_PRIME | chr9 | 37861684 | ||||
chr9:37861797
|
C | A | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*289C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 289 | chr9 | 37861797 | |||||
chr9:37862004
|
T | G | 1 | a0001c0001t0034 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 496 | chr9 | 37862004 | |||||
chr9:37862069
|
A | G | 1 | a0001c0001t0058 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 561 | chr9 | 37862069 | |||||
chr9:37862127
|
A | T | 10 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(7): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*619A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 619 | chr9 | 37862127 | |||||
chr9:37862181
|
A | T | 10 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(7): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*673A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 673 | chr9 | 37862181 | |||||
chr9:37862632
|
G | A | 1 | a0001c0001t0018 | 2 | HG02976.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1124 | chr9 | 37862632 | |||||
chr9:37862781
|
G | A | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1273G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1273 | chr9 | 37862781 | |||||
chr9:37862871
|
A | G | 1 | a0001c0001t0057 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1363A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1363 | chr9 | 37862871 | |||||
chr9:37863065
|
T | C | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1557T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1557 | chr9 | 37863065 | |||||
chr9:37863152
|
G | C | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1644G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1644 | chr9 | 37863152 | |||||
chr9:37863171
|
C | T | 1 | a0001c0001t0056 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1663 | chr9 | 37863171 | |||||
chr9:37863199
|
A | G | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1691A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1691 | chr9 | 37863199 | |||||
chr9:37863228
|
A | G | 1 | a0001c0001t0055 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1720A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1720 | chr9 | 37863228 | |||||
chr9:37863262
|
G | C | 2 | a0001c0001t0013a0001c0001t0018 | 6 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1754G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1754 | chr9 | 37863262 | |||||
chr9:37863275
|
G | A | 4 | a0001c0001t0008a0001c0001t0018a0001c0003t0030others(1): Show | 10 | HG02451.hp2 HG02717.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1767G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1767 | chr9 | 37863275 | |||||
chr9:37863325
|
C | CA | 8 | a0001c0001t0006a0001c0001t0010a0001c0001t0023others(5): Show | 21 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1841dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
C | CAAAA | 6 | a0001c0001t0019a0001c0001t0020a0001c0001t0021others(3): Show | 9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1838_*1841dupAAAA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005a0001c0001t0028 | 13 | HG01081.hp1 HG01168.hp1 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1830_*1841dupAAAA others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0009a0001c0001t0060a0001c0001t0061 | 8 | HG01123.hp2 HG03831.hp1 HG04199.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1829_*1841dupAAAA others(9): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0027 | 2 | NA18957.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1828_*1841dupAAAA others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0059 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1827_*1841dupAAAA others(11): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
C | CAAAAAAA others(10): Show |
1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1825_*1841dupAAAA others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
CA | C | 6 | a0001c0001t0017a0001c0001t0050a0001c0001t0051others(3): Show | 8 | HG02965.hp1 HG02965.hp2 HG03491.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1841delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1841 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863325
|
CAAA | C | 3 | a0001c0001t0008a0001c0001t0018a0003c0007t0008 | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1839_*1841delAAA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1839 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | ||||
chr9:37863357
|
C | T | 1 | a0001c0001t0049 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1849C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1849 | chr9 | 37863357 | |||||
chr9:37863482
|
A | G | 1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1974A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1974 | chr9 | 37863482 | |||||
chr9:37863648
|
T | C | 6 | a0001c0001t0019a0001c0001t0020a0001c0001t0021others(3): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2140T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2140 | chr9 | 37863648 | |||||
chr9:37863893
|
G | T | 3 | a0001c0001t0011a0001c0001t0048a0001c0001t0054 | 7 | NA18946.hp1 NA18955.hp1 NA18974.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2385G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2385 | chr9 | 37863893 | |||||
chr9:37863958
|
T | C | 1 | a0001c0001t0035 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2450T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2450 | chr9 | 37863958 | |||||
chr9:37864022
|
AC | A | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(5): Show | 73 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2515delC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2515 | chr9 | 37864022 | |||||
chr9:37864060
|
A | C | 1 | a0001c0001t0021 | 2 | HG01243.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2552A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2552 | chr9 | 37864060 | |||||
chr9:37864097
|
G | A | 2 | a0001c0001t0024a0001c0001t0050 | 3 | HG00140.hp1 HG02738.hp1 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2589G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2589 | chr9 | 37864097 | |||||
chr9:37864163
|
G | A | 1 | a0001c0001t0040 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2655G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2655 | chr9 | 37864163 | |||||
chr9:37864234
|
C | G | 1 | a0001c0001t0038 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2726C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2726 | chr9 | 37864234 | |||||
chr9:37864239
|
T | A | 2 | a0001c0001t0022a0001c0001t0031 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2731T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2731 | chr9 | 37864239 | |||||
chr9:37864265
|
A | G | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2757A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2757 | chr9 | 37864265 | |||||
chr9:37864477
|
A | C | 1 | a0001c0001t0063 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2969A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2969 | chr9 | 37864477 | |||||
chr9:37864478
|
G | T | 1 | a0001c0001t0063 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2970G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2970 | chr9 | 37864478 | |||||
chr9:37864533
|
G | A | 1 | a0001c0001t0028 | 2 | HG01081.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3025G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3025 | chr9 | 37864533 | |||||
chr9:37864539
|
G | A | 2 | a0001c0001t0025a0001c0001t0051 | 3 | HG02717.hp2 HG02965.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3031G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3031 | chr9 | 37864539 | |||||
chr9:37864542
|
C | T | 1 | a0001c0001t0061 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3034C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3034 | chr9 | 37864542 | |||||
chr9:37864583
|
C | CA | 5 | a0001c0001t0019a0001c0001t0020a0001c0001t0032others(2): Show | 7 | HG02486.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3092dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3093 | INFO_REALIGN_3_PRIME | chr9 | 37864583 | ||||
chr9:37864596
|
A | AT | 17 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(14): Show | 47 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3088_*3089insT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3089 | chr9 | 37864596 | |||||
chr9:37864596
|
A | T | 13 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(10): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3088A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3088 | chr9 | 37864596 | |||||
chr9:37864597
|
A | T | 7 | a0001c0001t0003a0001c0001t0035a0001c0001t0037others(4): Show | 45 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3089A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3089 | chr9 | 37864597 | |||||
chr9:37865058
|
T | C | 10 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(7): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3550T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3550 | chr9 | 37865058 | |||||
chr9:37865307
|
C | G | 4 | a0001c0001t0008a0001c0001t0018a0001c0003t0030others(1): Show | 10 | HG02451.hp2 HG02717.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3799C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3799 | chr9 | 37865307 | |||||
chr9:37865409
|
T | C | 1 | a0001c0001t0033 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3901T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3901 | chr9 | 37865409 | |||||
chr9:37865590
|
T | G | 1 | a0001c0001t0060 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4082T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4082 | chr9 | 37865590 | |||||
chr9:37865754
|
G | A | 5 | a0001c0001t0019a0001c0001t0020a0001c0001t0021others(2): Show | 9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4246G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4246 | chr9 | 37865754 | |||||
chr9:37865795
|
A | G | 1 | a0001c0001t0046 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4287A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4287 | chr9 | 37865795 | |||||
chr9:37865822
|
TAAGAA | T | 1 | a0001c0001t0014 | 4 | HG03209.hp2 HG03540.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4318_*4322delAAAA others(1): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4318 | INFO_REALIGN_3_PRIME | chr9 | 37865822 | ||||
chr9:37865907
|
T | C | 1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4399T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4399 | chr9 | 37865907 | |||||
chr9:37865946
|
A | G | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(19): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*4438A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4438 | chr9 | 37865946 | |||||
chr9:37866010
|
G | A | 1 | a0001c0001t0058 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4502G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4502 | chr9 | 37866010 | |||||
chr9:37866024
|
G | A | 1 | a0001c0001t0036 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4516G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4516 | chr9 | 37866024 | |||||
chr9:37866065
|
A | G | 1 | a0001c0001t0041 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4557A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4557 | chr9 | 37866065 | |||||
chr9:37866222
|
T | C | 1 | a0001c0001t0043 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4714T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4714 | chr9 | 37866222 | |||||
chr9:37866528
|
G | A | 1 | a0001c0001t0026 | 2 | HG00639.hp2 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5020G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5020 | chr9 | 37866528 | |||||
chr9:37866554
|
C | T | 10 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(7): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5046C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5046 | chr9 | 37866554 | |||||
chr9:37866556
|
A | G | 1 | a0001c0001t0044 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5048A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5048 | chr9 | 37866556 | |||||
chr9:37866590
|
C | T | 1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5082C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5082 | chr9 | 37866590 | |||||
chr9:37866635
|
G | A | 10 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(7): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5127G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5127 | chr9 | 37866635 | |||||
chr9:37867036
|
A | C | 1 | a0001c0001t0016 | 3 | HG00741.hp1 HG01106.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5528A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5528 | chr9 | 37867036 | |||||
chr9:37867110
|
T | C | 3 | a0001c0001t0039a0001c0001t0045a0001c0004t0047 | 3 | HG02074.hp1 HG02155.hp1 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5602T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5602 | chr9 | 37867110 | |||||
chr9:37867194
|
T | C | 19 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(16): Show | 50 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5686T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5686 | chr9 | 37867194 | |||||
chr9:37867321
|
T | C | 2 | a0001c0001t0022a0001c0001t0031 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5813T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5813 | chr9 | 37867321 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:37801447
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+42G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801447 | ||||||
chr9:37801462
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+57G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801462 | ||||||
chr9:37801465
|
C | T | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.539+60C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801465 | ||||||
chr9:37801488
|
G | C | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+83G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801488 | ||||||
chr9:37801717
|
G | C | 4 | a0001c0001t0004g0058a0001c0001t0013g0056a0001c0001t0013g0057others(1): Show | 4 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+312G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801717 | ||||||
chr9:37801815
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.539+410C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801815 | ||||||
chr9:37801859
|
C | T | 1 | a0001c0001t0004g0343 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.539+454C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801859 | ||||||
chr9:37802177
|
A | T | 1 | a0001c0001t0001g0344 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.539+772A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802177 | ||||||
chr9:37802237
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.539+832A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802237 | ||||||
chr9:37802455
|
T | C | 1 | a0001c0001t0002g0060 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.539+1050T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802455 | ||||||
chr9:37802665
|
A | G | 1 | a0001c0001t0038g0340 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.539+1260A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802665 | ||||||
chr9:37802761
|
A | G | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+1356A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802761 | ||||||
chr9:37802868
|
C | G | 1 | a0001c0001t0034g0339 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.539+1463C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802868 | ||||||
chr9:37803213
|
T | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.539+1808T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803213 | ||||||
chr9:37803300
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.539+1895T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803300 | ||||||
chr9:37803412
|
TTTTATA | T | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+2015_539+2020d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37803412 | |||||
chr9:37803527
|
C | T | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+2122C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803527 | ||||||
chr9:37803894
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02647.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.539+2489T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803894 | ||||||
chr9:37803951
|
G | A | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.539+2546G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803951 | ||||||
chr9:37803989
|
A | G | 1 | a0001c0001t0019g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.539+2584A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803989 | ||||||
chr9:37804028
|
T | C | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+2623T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804028 | ||||||
chr9:37804036
|
A | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+2631A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804036 | ||||||
chr9:37804040
|
A | G | 1 | a0001c0001t0019g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.539+2635A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804040 | ||||||
chr9:37804194
|
AAC | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.539+2793_539+2794d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37804194 | |||||
chr9:37804356
|
A | G | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.539+2951A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804356 | ||||||
chr9:37804439
|
T | G | 29 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+3034T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804439 | ||||||
chr9:37804519
|
G | A | 1 | a0001c0001t0015g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.539+3114G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804519 | ||||||
chr9:37804546
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00733.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.539+3141G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804546 | ||||||
chr9:37804598
|
G | A | 4 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+3193G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804598 | ||||||
chr9:37804716
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+3311C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804716 | ||||||
chr9:37804846
|
C | A | 7 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+3441C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804846 | ||||||
chr9:37804871
|
G | C | 2 | a0001c0001t0020g0048a0001c0001t0020g0049 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.539+3466G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804871 | ||||||
chr9:37804881
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+3476C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804881 | ||||||
chr9:37804957
|
G | T | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+3552G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804957 | ||||||
chr9:37804958
|
A | T | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+3553A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804958 | ||||||
chr9:37805007
|
A | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.539+3602A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805007 | ||||||
chr9:37805196
|
G | A | 1 | a0001c0001t0060g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.539+3791G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805196 | ||||||
chr9:37805327
|
C | CA | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+3929dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37805327 | |||||
chr9:37805343
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+3938G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805343 | ||||||
chr9:37805432
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+4027G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805432 | ||||||
chr9:37805653
|
A | G | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+4248A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805653 | ||||||
chr9:37805822
|
C | T | 7 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+4417C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805822 | ||||||
chr9:37805954
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+4549G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805954 | ||||||
chr9:37806009
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+4604G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806009 | ||||||
chr9:37806028
|
G | A | 17 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(14): Show | 17 | HG00621.hp2 HG02071.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.539+4623G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806028 | ||||||
chr9:37806094
|
A | T | 4 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(1): Show | 4 | HG03942.hp2 HG04115.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+4689A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806094 | ||||||
chr9:37806248
|
T | C | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+4843T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806248 | ||||||
chr9:37806428
|
A | C | 51 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(48): Show | 53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+5023A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806428 | ||||||
chr9:37806465
|
C | T | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+5060C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806465 | ||||||
chr9:37806497
|
C | G | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+5092C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806497 | ||||||
chr9:37806580
|
T | C | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+5175T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806580 | ||||||
chr9:37806633
|
T | C | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.539+5228T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806633 | ||||||
chr9:37806894
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | NA18968.hp1 NA18988.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+5489A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806894 | ||||||
chr9:37807061
|
C | A | 51 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(48): Show | 53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+5656C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807061 | ||||||
chr9:37807064
|
T | C | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+5659T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807064 | ||||||
chr9:37807225
|
T | G | 1 | a0001c0001t0010g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.539+5820T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807225 | ||||||
chr9:37807275
|
T | G | 1 | a0001c0001t0004g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.539+5870T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807275 | ||||||
chr9:37807287
|
T | C | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.539+5882T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807287 | ||||||
chr9:37807570
|
T | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.539+6165T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807570 | ||||||
chr9:37807621
|
T | C | 1 | a0001c0001t0062g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.539+6216T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807621 | ||||||
chr9:37807653
|
CTTTTCTT others(3): Show |
C | 4 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+6253_539+6262d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37807653 | |||||
chr9:37807658
|
CT | C | 284 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.539+6274delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37807658 | |||||
chr9:37807658
|
CTT | C | 8 | a0001c0001t0001g0067a0001c0001t0001g0087a0001c0001t0001g0090others(5): Show | 8 | HG01169.hp2 HG03209.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+6273_539+6274d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37807658 | |||||
chr9:37807773
|
C | T | 2 | a0001c0001t0017g0327a0001c0001t0017g0328 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.539+6368C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807773 | ||||||
chr9:37807823
|
C | T | 80 | a0001c0001t0001g0261a0001c0001t0001g0281a0001c0001t0001g0320others(77): Show | 80 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.539+6418C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807823 | ||||||
chr9:37807824
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+6419G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807824 | ||||||
chr9:37807906
|
C | G | 1 | a0001c0001t0004g0251 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.539+6501C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807906 | ||||||
chr9:37808049
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.539+6644A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808049 | ||||||
chr9:37808118
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0250 | 3 | HG01081.hp2 HG01243.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.539+6713C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808118 | ||||||
chr9:37808153
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.539+6748A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808153 | ||||||
chr9:37808214
|
A | C | 1 | a0001c0001t0002g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.539+6809A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808214 | ||||||
chr9:37808463
|
T | A | 2 | a0001c0001t0027g0014a0001c0001t0027g0015 | 2 | NA18957.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.539+7058T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808463 | ||||||
chr9:37808464
|
A | T | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0010g0245 | 3 | NA18943.hp1 NA18947.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.539+7059A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808464 | ||||||
chr9:37808473
|
T | TATATATT others(25): Show |
1 | a0001c0001t0003g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539+7088_539+7119d others(34): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808473 | |||||
chr9:37808505
|
C | T | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+7100C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808505 | ||||||
chr9:37808505
|
CAT | C | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.539+7105_539+7106d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808505 | |||||
chr9:37808513
|
TATATA | T | 5 | a0001c0001t0002g0336a0001c0001t0012g0002a0001c0001t0012g0054others(2): Show | 6 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+7114_539+7118d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808513 | |||||
chr9:37808524
|
T | TAAATATA others(20): Show |
1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+7119_539+7120i others(29): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808524 | ||||||
chr9:37808524
|
T | TAAATATA others(52): Show |
29 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+7119_539+7120i others(61): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808524 | ||||||
chr9:37808572
|
T | C | 1 | a0001c0001t0006g0252 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.539+7167T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808572 | ||||||
chr9:37808610
|
A | AATATAAT others(31): Show |
7 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+7222_539+7223i others(40): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808610 | |||||
chr9:37808628
|
A | T | 37 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(34): Show | 37 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.539+7223A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808628 | ||||||
chr9:37808637
|
TA | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG02155.hp2 NA18959.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+7237delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808637 | |||||
chr9:37808642
|
A | ATATAT | 277 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(274): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.539+7238_539+7242d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808642 | |||||
chr9:37808642
|
A | ATATATTA others(23): Show |
4 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0004g0239others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+7242_539+7243i others(32): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808642 | |||||
chr9:37808733
|
AAT | A | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+7334_539+7335d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808733 | |||||
chr9:37808748
|
A | ATATATAA others(138): Show |
1 | a0001c0001t0003g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(147): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(157): Show |
1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(166): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(148): Show |
1 | a0001c0001t0014g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(157): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(153): Show |
90 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(87): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(162): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(155): Show |
1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(164): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(155): Show |
2 | a0001c0001t0001g0246a0001c0001t0010g0245 | 2 | NA18943.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(164): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(154): Show |
1 | a0001c0001t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(163): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(155): Show |
182 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0061others(179): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(164): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(150): Show |
4 | a0001c0001t0002g0091a0001c0001t0002g0317a0001c0001t0002g0318others(1): Show | 4 | HG00558.hp1 NA18971.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(159): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(154): Show |
1 | a0001c0001t0001g0244 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(163): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(153): Show |
2 | a0001c0001t0001g0320a0001c0001t0002g0321 | 2 | HG02080.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(162): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(156): Show |
2 | a0001c0001t0002g0323a0001c0001t0006g0322 | 2 | HG01978.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(165): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(154): Show |
9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG01069.hp2 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(163): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(237): Show |
1 | a0001c0001t0008g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(246): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(176): Show |
1 | a0001c0001t0005g0016 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(185): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(191): Show |
2 | a0001c0001t0005g0018a0001c0001t0009g0017 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(200): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(208): Show |
4 | a0001c0001t0015g0010a0001c0001t0015g0019a0001c0001t0060g0011others(1): Show | 4 | HG01123.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(217): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(207): Show |
13 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0023others(10): Show | 13 | HG01081.hp1 HG01168.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(216): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(195): Show |
1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(204): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(234): Show |
1 | a0001c0001t0008g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(243): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(238): Show |
3 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0008g0044 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(247): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(77): Show |
4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(86): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(107): Show |
9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(116): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(207): Show |
1 | a0001c0001t0015g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(216): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(206): Show |
8 | a0001c0001t0009g0013a0001c0001t0009g0033a0001c0001t0009g0036others(5): Show | 8 | HG04184.hp2 NA18948.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(215): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(223): Show |
1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(232): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37808748
|
A | ATATATAA others(202): Show |
1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(211): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | |||||
chr9:37809093
|
G | GAA | 46 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(43): Show | 48 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.539+7702_539+7703d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809093 | |||||
chr9:37809124
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0010g0245 | 2 | NA18943.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.539+7719C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37809124 | ||||||
chr9:37809394
|
TA | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0078others(31): Show | 38 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.539+8003delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809394 | |||||
chr9:37809394
|
TAA | T | 6 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+8002_539+8003d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809394 | |||||
chr9:37809394
|
TAAAA | T | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+8000_539+8003d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809394 | |||||
chr9:37809903
|
C | T | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+8498C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37809903 | ||||||
chr9:37809996
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+8591C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37809996 | ||||||
chr9:37810152
|
T | TA | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0006g0253others(5): Show | 8 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.539+8761dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37810152 | |||||
chr9:37810152
|
TA | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0200a0001c0001t0004g0120others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+8761delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37810152 | |||||
chr9:37810396
|
G | T | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.540-8892G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810396 | ||||||
chr9:37810459
|
C | CTT | 29 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.540-8827_540-8826d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37810459 | |||||
chr9:37810463
|
C | T | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.540-8825C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810463 | ||||||
chr9:37810467
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(85): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.540-8821T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810467 | ||||||
chr9:37810525
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-8763A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810525 | ||||||
chr9:37810859
|
C | T | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.540-8429C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810859 | ||||||
chr9:37810929
|
C | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-8359C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810929 | ||||||
chr9:37811137
|
C | G | 1 | a0001c0001t0003g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.540-8151C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811137 | ||||||
chr9:37811224
|
C | T | 1 | a0001c0001t0008g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540-8064C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811224 | ||||||
chr9:37811291
|
CACT | C | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-7994_540-7992d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37811291 | |||||
chr9:37811303
|
G | A | 4 | a0001c0001t0014g0088a0001c0001t0014g0129a0001c0001t0014g0201others(1): Show | 4 | HG03209.hp2 HG03540.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-7985G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811303 | ||||||
chr9:37811407
|
G | A | 3 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0008g0044 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.540-7881G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811407 | ||||||
chr9:37811462
|
T | C | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-7826T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811462 | ||||||
chr9:37811772
|
GA | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(14): Show | 19 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.540-7513delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37811772 | |||||
chr9:37811815
|
A | G | 1 | a0001c0001t0053g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540-7473A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811815 | ||||||
chr9:37811956
|
G | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-7332G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811956 | ||||||
chr9:37811991
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.540-7297A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811991 | ||||||
chr9:37812169
|
CCTT | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(89): Show | 95 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.540-7116_540-7114d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37812169 | |||||
chr9:37812317
|
A | G | 1 | a0001c0001t0007g0316 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.540-6971A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812317 | ||||||
chr9:37812342
|
T | A | 1 | a0001c0001t0001g0261 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-6946T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812342 | ||||||
chr9:37812343
|
A | T | 1 | a0001c0001t0001g0261 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-6945A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812343 | ||||||
chr9:37812561
|
G | A | 79 | a0001c0001t0001g0281a0001c0001t0001g0320a0001c0001t0002g0091others(76): Show | 79 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.540-6727G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812561 | ||||||
chr9:37812612
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-6676G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812612 | ||||||
chr9:37812706
|
T | A | 1 | a0001c0001t0001g0095 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.540-6582T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812706 | ||||||
chr9:37812752
|
G | C | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-6536G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812752 | ||||||
chr9:37812792
|
G | A | 1 | a0001c0001t0004g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.540-6496G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812792 | ||||||
chr9:37812792
|
G | T | 2 | a0001c0001t0001g0227a0001c0001t0023g0089 | 2 | HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.540-6496G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812792 | ||||||
chr9:37812794
|
T | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0066others(13): Show | 17 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.540-6494T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812794 | ||||||
chr9:37812865
|
A | G | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-6423A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812865 | ||||||
chr9:37813732
|
A | G | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-5556A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37813732 | ||||||
chr9:37813735
|
A | C | 1 | a0001c0001t0031g0347 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.540-5553A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37813735 | ||||||
chr9:37814018
|
A | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 26 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.540-5270A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814018 | ||||||
chr9:37814054
|
T | C | 79 | a0001c0001t0001g0281a0001c0001t0001g0320a0001c0001t0002g0091others(76): Show | 79 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.540-5234T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814054 | ||||||
chr9:37814080
|
C | CTA | 33 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0101others(30): Show | 33 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.540-5162_540-5161d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATA | 33 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0071others(30): Show | 34 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.540-5164_540-5161d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATA | 19 | a0001c0001t0001g0122a0001c0001t0001g0222a0001c0001t0001g0247others(16): Show | 20 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.540-5166_540-5161d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATAT others(1): Show |
20 | a0001c0001t0001g0068a0001c0001t0001g0121a0001c0001t0001g0206others(17): Show | 20 | HG01074.hp1 HG01099.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.540-5168_540-5161d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATAT others(3): Show |
7 | a0001c0001t0001g0205a0001c0001t0002g0273a0001c0001t0003g0134others(4): Show | 7 | HG00099.hp1 HG00438.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-5170_540-5161d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATAT others(5): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0267others(7): Show | 10 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-5172_540-5161d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATAT others(7): Show |
3 | a0001c0001t0003g0131a0001c0001t0007g0265a0001c0001t0055g0264 | 3 | HG01071.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.540-5174_540-5161d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATAT others(9): Show |
1 | a0001c0001t0002g0263 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.540-5176_540-5161d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
C | CTATATAT others(11): Show |
1 | a0001c0001t0045g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.540-5178_540-5161d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTA | C | 32 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0094others(29): Show | 32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.540-5162_540-5161d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATA | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0080others(26): Show | 30 | HG00323.hp2 HG00558.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.540-5164_540-5161d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATA | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 20 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.540-5166_540-5161d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(1): Show |
C | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0078others(2): Show | 6 | HG00621.hp2 HG01243.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-5168_540-5161d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(3): Show |
C | 10 | a0001c0001t0001g0090a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG01516.hp2 HG01993.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-5170_540-5161d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(5): Show |
C | 7 | a0001c0001t0001g0193a0001c0001t0004g0192a0001c0001t0009g0037others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-5172_540-5161d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(7): Show |
C | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG00597.hp2 HG02155.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-5174_540-5161d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(9): Show |
C | 1 | a0001c0001t0032g0050 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.540-5176_540-5161d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(11): Show |
C | 6 | a0001c0001t0001g0067a0001c0001t0004g0058a0001c0001t0013g0057others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-5178_540-5161d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(13): Show |
C | 8 | a0001c0001t0002g0314a0001c0001t0004g0239a0001c0001t0012g0002others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-5180_540-5161d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(19): Show |
C | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.540-5186_540-5161d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(21): Show |
C | 1 | a0001c0001t0002g0315 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.540-5188_540-5161d others(30): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814080
|
CTATATAT others(23): Show |
C | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-5190_540-5161d others(32): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | |||||
chr9:37814107
|
TATATATA others(10): Show |
T | 2 | a0001c0001t0005g0038a0001c0001t0015g0019 | 2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.540-5180_540-5164d others(19): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814107 | ||||||
chr9:37814109
|
TATATATA others(8): Show |
T | 25 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(22): Show | 25 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.540-5178_540-5164d others(17): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814109 | ||||||
chr9:37814111
|
TATATATA others(6): Show |
T | 2 | a0001c0001t0027g0014a0001c0001t0063g0039 | 2 | HG01496.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.540-5176_540-5164d others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814111 | ||||||
chr9:37814119
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0008g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.540-5168_540-5158d others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814119 | ||||||
chr9:37814119
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0060 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.540-5168_540-5155d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814119 | ||||||
chr9:37814122
|
A | T | 8 | a0001c0001t0009g0037a0001c0001t0019g0051a0001c0001t0019g0052others(5): Show | 9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-5166A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814122 | ||||||
chr9:37814124
|
A | G | 8 | a0001c0001t0009g0037a0001c0001t0019g0051a0001c0001t0019g0052others(5): Show | 9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-5164A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814124 | ||||||
chr9:37814124
|
A | T | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.540-5164A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814124 | ||||||
chr9:37814125
|
TATTTG | T | 3 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0008g0044 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.540-5162_540-5158d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814125 | ||||||
chr9:37814126
|
A | G | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.540-5162A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814126 | ||||||
chr9:37814126
|
A | T | 38 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(35): Show | 39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.540-5162A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814126 | ||||||
chr9:37814127
|
T | G | 38 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(35): Show | 39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.540-5161T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | ||||||
chr9:37814127
|
T | TATATATA others(4): Show |
1 | a0001c0001t0002g0266 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540-5161_540-5160i others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | ||||||
chr9:37814127
|
T | TATATATA others(6): Show |
1 | a0001c0001t0018g0341 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.540-5161_540-5160i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | ||||||
chr9:37814127
|
T | TATATATA others(4): Show |
2 | a0001c0001t0003g0143a0001c0001t0018g0342 | 2 | HG04204.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-5161_540-5160i others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | ||||||
chr9:37814129
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.540-5159T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814129 | ||||||
chr9:37814130
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.540-5158G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814130 | ||||||
chr9:37814192
|
G | T | 1 | a0001c0001t0014g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540-5096G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814192 | ||||||
chr9:37814201
|
C | T | 1 | a0001c0001t0001g0008 | 2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.540-5087C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814201 | ||||||
chr9:37814241
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.540-5047C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814241 | ||||||
chr9:37814301
|
C | CT | 28 | a0001c0001t0001g0077a0001c0001t0001g0114a0001c0001t0001g0126others(25): Show | 28 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.540-4966dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814301 | |||||
chr9:37814301
|
CT | C | 39 | a0001c0001t0001g0241a0001c0001t0005g0016a0001c0001t0005g0018others(36): Show | 40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.540-4966delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814301 | |||||
chr9:37814301
|
CTT | C | 7 | a0001c0001t0008g0042a0001c0001t0008g0044a0001c0001t0008g0045others(4): Show | 7 | HG01496.hp2 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-4967_540-4966d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814301 | |||||
chr9:37814452
|
A | G | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-4836A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814452 | ||||||
chr9:37814495
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-4793A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814495 | ||||||
chr9:37814704
|
G | T | 1 | a0001c0001t0037g0187 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.540-4584G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814704 | ||||||
chr9:37814722
|
T | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-4566T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814722 | ||||||
chr9:37814876
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.540-4412C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814876 | ||||||
chr9:37814950
|
T | C | 1 | a0001c0001t0040g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.540-4338T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814950 | ||||||
chr9:37815017
|
T | C | 1 | a0001c0001t0003g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.540-4271T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815017 | ||||||
chr9:37815204
|
C | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-4084C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815204 | ||||||
chr9:37815306
|
T | A | 3 | a0001c0001t0004g0058a0001c0001t0013g0057a0001c0001t0013g0059 | 3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.540-3982T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815306 | ||||||
chr9:37815380
|
C | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-3908C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815380 | ||||||
chr9:37815443
|
G | A | 1 | a0001c0001t0012g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540-3845G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815443 | ||||||
chr9:37815517
|
C | T | 1 | a0001c0001t0014g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540-3771C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815517 | ||||||
chr9:37815541
|
A | T | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-3747A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815541 | ||||||
chr9:37815547
|
C | T | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-3741C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815547 | ||||||
chr9:37815606
|
T | C | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-3682T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815606 | ||||||
chr9:37815633
|
A | AAAACTCT others(3): Show |
1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540-3648_540-3647i others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815633 | |||||
chr9:37815649
|
T | TA | 41 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(38): Show | 42 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-3627dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815649 | |||||
chr9:37815667
|
A | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-3621A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815667 | ||||||
chr9:37815711
|
A | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.540-3577A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815711 | ||||||
chr9:37815719
|
TAATAG | T | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-3563_540-3559d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815719 | |||||
chr9:37815736
|
C | T | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-3552C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815736 | ||||||
chr9:37815810
|
T | G | 1 | a0001c0001t0008g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540-3478T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815810 | ||||||
chr9:37815883
|
TC | T | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-3402delC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815883 | |||||
chr9:37815926
|
T | C | 1 | a0001c0001t0025g0173 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.540-3362T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815926 | ||||||
chr9:37815975
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.540-3313G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815975 | ||||||
chr9:37816064
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-3224A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816064 | ||||||
chr9:37816129
|
T | TA | 43 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(40): Show | 45 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.540-3150dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816129 | |||||
chr9:37816129
|
T | TAA | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-3151_540-3150d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816129 | |||||
chr9:37816343
|
C | A | 1 | a0001c0001t0019g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540-2945C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816343 | ||||||
chr9:37816498
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.540-2790G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816498 | ||||||
chr9:37816590
|
CA | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-2689delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816590 | |||||
chr9:37816659
|
G | GGGGGGGG others(13): Show |
4 | a0001c0001t0009g0013a0001c0001t0009g0033a0001c0001t0027g0014others(1): Show | 4 | NA18957.hp1 NA18960.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGGG others(18): Show |
1 | a0001c0001t0059g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.540-2628_540-2627i others(27): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGGG others(7): Show |
1 | a0001c0001t0061g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGGG others(11): Show |
1 | a0001c0001t0015g0035 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.540-2628_540-2627i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGGG others(13): Show |
2 | a0001c0001t0009g0036a0001c0001t0009g0037 | 2 | NA18965.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGTG others(7): Show |
2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | NA18968.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGTG others(9): Show |
2 | a0001c0001t0005g0023a0001c0001t0009g0022 | 2 | HG04199.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGTG others(11): Show |
2 | a0001c0001t0005g0024a0001c0001t0015g0032 | 2 | HG03209.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGTG others(13): Show |
4 | a0001c0001t0005g0016a0001c0001t0005g0025a0001c0001t0005g0026others(1): Show | 4 | HG01515.hp1 HG02300.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGGTG others(15): Show |
3 | a0001c0001t0005g0031a0001c0001t0028g0027a0001c0001t0028g0028 | 3 | HG01081.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGGTGT others(10): Show |
1 | a0001c0001t0015g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(19): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGTGTG others(7): Show |
1 | a0001c0001t0009g0017 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGTGTG others(9): Show |
1 | a0001c0001t0005g0029 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGTGTG others(11): Show |
3 | a0001c0001t0005g0018a0001c0001t0005g0038a0001c0001t0063g0039 | 3 | HG01496.hp2 NA19004.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGTGTG others(13): Show |
1 | a0001c0001t0060g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGGGTGTG others(21): Show |
1 | a0001c0001t0015g0019 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(30): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGT | 30 | a0001c0001t0001g0009a0001c0001t0001g0113a0001c0001t0001g0117others(27): Show | 32 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.540-2598_540-2597d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGTGT | 21 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0001t0001g0235others(18): Show | 23 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.540-2600_540-2597d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGTGTGT | 8 | a0001c0001t0008g0041a0001c0001t0008g0046a0001c0001t0019g0051others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.540-2602_540-2597d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGTGTGTG others(1): Show |
5 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0012g0002others(2): Show | 6 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-2604_540-2597d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816659
|
G | GGTGTGTG others(3): Show |
2 | a0001c0001t0008g0044a0001c0001t0012g0054 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.540-2606_540-2597d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | |||||
chr9:37816661
|
T | G | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0344others(3): Show | 6 | HG00140.hp1 HG01074.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-2627T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816661 | ||||||
chr9:37816884
|
A | G | 1 | a0001c0001t0061g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.540-2404A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816884 | ||||||
chr9:37816930
|
A | C | 7 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-2358A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816930 | ||||||
chr9:37816963
|
C | T | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-2325C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816963 | ||||||
chr9:37817033
|
T | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540-2255T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817033 | ||||||
chr9:37817082
|
G | C | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-2206G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817082 | ||||||
chr9:37817178
|
C | A | 1 | a0001c0001t0009g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.540-2110C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817178 | ||||||
chr9:37817198
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.540-2090T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817198 | ||||||
chr9:37817226
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.540-2062C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817226 | ||||||
chr9:37817279
|
A | G | 1 | a0001c0001t0009g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.540-2009A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817279 | ||||||
chr9:37817353
|
C | A | 5 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(2): Show | 5 | HG02451.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-1935C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817353 | ||||||
chr9:37817467
|
G | A | 1 | a0001c0001t0002g0296 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.540-1821G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817467 | ||||||
chr9:37817592
|
CGTCTCAG others(19): Show |
C | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-1691_540-1666d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37817592 | |||||
chr9:37817593
|
G | A | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-1695G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817593 | ||||||
chr9:37817687
|
G | A | 1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.540-1601G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817687 | ||||||
chr9:37817717
|
A | G | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-1571A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817717 | ||||||
chr9:37817738
|
C | CA | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-1540dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37817738 | |||||
chr9:37817904
|
A | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-1384A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817904 | ||||||
chr9:37817935
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-1353G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817935 | ||||||
chr9:37818037
|
T | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-1251T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818037 | ||||||
chr9:37818282
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0006g0253a0001c0001t0006g0254others(2): Show | 5 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-1006C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818282 | ||||||
chr9:37818290
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.540-998G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818290 | ||||||
chr9:37818481
|
TAATC | T | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-804_540-801del others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37818481 | |||||
chr9:37818596
|
C | T | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-692C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818596 | ||||||
chr9:37818723
|
T | C | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-565T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818723 | ||||||
chr9:37818733
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540-555G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818733 | ||||||
chr9:37819008
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.540-280T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37819008 | ||||||
chr9:37819062
|
G | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-226G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37819062 | ||||||
chr9:37819149
|
A | C | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.540-139A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37819149 | ||||||
chr9:37819178
|
CA | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-99delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37819178 | |||||
chr9:37819525
|
T | C | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+124T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819525 | ||||||
chr9:37819684
|
T | C | 2 | a0001c0001t0019g0051a0001c0001t0019g0052 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.653+283T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819684 | ||||||
chr9:37819732
|
T | A | 1 | a0001c0001t0016g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.653+331T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819732 | ||||||
chr9:37819790
|
T | C | 29 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.653+389T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819790 | ||||||
chr9:37819909
|
T | G | 1 | a0001c0001t0002g0270 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.653+508T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819909 | ||||||
chr9:37819996
|
T | TAGG | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+597_653+598ins others(3): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37819996 | |||||
chr9:37820127
|
T | C | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.653+726T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820127 | ||||||
chr9:37820143
|
A | G | 9 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+742A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820143 | ||||||
chr9:37820226
|
T | A | 1 | a0001c0001t0003g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.653+825T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820226 | ||||||
chr9:37820397
|
A | G | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 9 | HG01069.hp2 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+996A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820397 | ||||||
chr9:37820416
|
C | T | 2 | a0001c0001t0002g0282a0001c0001t0007g0288 | 2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.653+1015C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820416 | ||||||
chr9:37820419
|
G | A | 92 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(89): Show | 95 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.653+1018G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820419 | ||||||
chr9:37820464
|
T | A | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+1063T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820464 | ||||||
chr9:37820515
|
A | C | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.653+1114A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820515 | ||||||
chr9:37820528
|
A | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+1127A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820528 | ||||||
chr9:37820691
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+1290G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820691 | ||||||
chr9:37820795
|
A | G | 74 | a0001c0001t0001g0281a0001c0001t0001g0320a0001c0001t0002g0091others(71): Show | 74 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.653+1394A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820795 | ||||||
chr9:37820820
|
A | G | 1 | a0001c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.653+1419A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820820 | ||||||
chr9:37820829
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(84): Show | 90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.653+1428C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820829 | ||||||
chr9:37821090
|
C | CAT | 13 | a0001c0001t0001g0281a0001c0001t0004g0239a0001c0001t0007g0265others(10): Show | 13 | HG02622.hp1 HG02965.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.653+1703_653+1704d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | |||||
chr9:37821090
|
C | CATATAT | 10 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(7): Show | 11 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+1699_653+1704d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | |||||
chr9:37821090
|
C | CATATATA others(1): Show |
4 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+1697_653+1704d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | |||||
chr9:37821090
|
C | CATATATA others(3): Show |
2 | a0001c0001t0008g0046a0001c0001t0063g0039 | 2 | HG01496.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.653+1695_653+1704d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | |||||
chr9:37821090
|
C | CATATATA others(11): Show |
1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.653+1704_653+1705i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | |||||
chr9:37821090
|
CAT | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(88): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.653+1703_653+1704d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | |||||
chr9:37821097
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.653+1696A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821097 | ||||||
chr9:37821104
|
T | TATATAC | 29 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.653+1704_653+1705i others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821104 | |||||
chr9:37821106
|
C | T | 11 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(8): Show | 12 | HG02451.hp2 HG02647.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.653+1705C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821106 | ||||||
chr9:37821125
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.653+1724A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821125 | ||||||
chr9:37821164
|
T | C | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+1763T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821164 | ||||||
chr9:37821179
|
C | T | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+1778C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821179 | ||||||
chr9:37821674
|
T | A | 1 | a0001c0001t0002g0297 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.653+2273T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821674 | ||||||
chr9:37821675
|
A | T | 2 | a0001c0001t0004g0239a0001c0001t0053g0240 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.653+2274A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821675 | ||||||
chr9:37822072
|
G | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+2671G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822072 | ||||||
chr9:37822073
|
C | T | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+2672C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822073 | ||||||
chr9:37822074
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+2673C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822074 | ||||||
chr9:37822268
|
A | G | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+2867A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822268 | ||||||
chr9:37822317
|
G | C | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+2916G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822317 | ||||||
chr9:37822353
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.653+2952C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822353 | ||||||
chr9:37822404
|
G | GAT | 16 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0001g0074others(13): Show | 17 | HG00621.hp2 HG01081.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.653+3040_653+3041d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATAT | 9 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0082others(6): Show | 9 | HG02132.hp2 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+3038_653+3041d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATAT | 5 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0001g0081others(2): Show | 5 | HG02055.hp2 HG02897.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+3036_653+3041d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(1): Show |
5 | a0001c0001t0003g0155a0001c0001t0003g0163a0001c0001t0003g0165others(2): Show | 5 | HG00642.hp1 HG02129.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+3034_653+3041d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(3): Show |
4 | a0001c0001t0001g0080a0001c0001t0003g0139a0001c0001t0003g0162others(1): Show | 4 | HG03710.hp2 HG03942.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+3032_653+3041d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(5): Show |
2 | a0001c0001t0003g0158a0001c0002t0004g0179 | 2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.653+3030_653+3041d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(7): Show |
4 | a0001c0001t0003g0134a0001c0001t0003g0138a0001c0001t0003g0147others(1): Show | 4 | HG01981.hp1 HG02602.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+3028_653+3041d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(9): Show |
7 | a0001c0001t0003g0137a0001c0001t0003g0146a0001c0001t0003g0148others(4): Show | 7 | HG00621.hp1 HG01975.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+3026_653+3041d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(11): Show |
5 | a0001c0001t0003g0084a0001c0001t0003g0144a0001c0001t0003g0161others(2): Show | 5 | HG00099.hp2 HG00438.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+3024_653+3041d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(13): Show |
5 | a0001c0001t0003g0083a0001c0001t0003g0131a0001c0001t0003g0164others(2): Show | 5 | HG00738.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+3022_653+3041d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(15): Show |
4 | a0001c0001t0003g0092a0001c0001t0003g0145a0001c0001t0037g0187others(1): Show | 4 | HG01361.hp1 HG02135.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+3020_653+3041d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
G | GATATATA others(17): Show |
3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0198 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.653+3018_653+3041d others(26): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GAT | G | 12 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0113others(9): Show | 12 | HG01123.hp1 HG01257.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.653+3040_653+3041d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATAT | G | 40 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0087others(37): Show | 40 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.653+3038_653+3041d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATAT | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0061a0001c0001t0001g0066others(36): Show | 40 | HG00323.hp1 HG00741.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.653+3036_653+3041d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATATA others(1): Show |
G | 5 | a0001c0001t0002g0060a0001c0001t0002g0282a0001c0001t0002g0289others(2): Show | 5 | HG02165.hp1 HG02523.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+3034_653+3041d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATATA others(3): Show |
G | 17 | a0001c0001t0002g0272a0001c0001t0002g0275a0001c0001t0002g0294others(14): Show | 17 | HG01255.hp1 HG01516.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.653+3032_653+3041d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATATA others(5): Show |
G | 59 | a0001c0001t0001g0281a0001c0001t0001g0320a0001c0001t0002g0091others(56): Show | 59 | HG00099.hp1 HG00558.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.653+3030_653+3041d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATATA others(7): Show |
G | 22 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(19): Show | 24 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.653+3028_653+3041d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATATA others(13): Show |
G | 9 | a0001c0001t0003g0004a0001c0001t0003g0166a0001c0001t0003g0171others(6): Show | 10 | HG00639.hp1 HG01074.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.653+3022_653+3041d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822404
|
GATATATA others(19): Show |
G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+3016_653+3041d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | |||||
chr9:37822576
|
T | C | 1 | a0001c0001t0061g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653+3175T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822576 | ||||||
chr9:37822605
|
G | T | 5 | a0001c0001t0004g0142a0001c0001t0023g0177a0001c0002t0004g0178others(2): Show | 5 | HG01109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+3204G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822605 | ||||||
chr9:37822638
|
A | C | 39 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(36): Show | 39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.653+3237A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822638 | ||||||
chr9:37822734
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+3333T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822734 | ||||||
chr9:37822762
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+3361G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822762 | ||||||
chr9:37822911
|
T | G | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.653+3510T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822911 | ||||||
chr9:37822941
|
T | G | 1 | a0001c0001t0009g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.653+3540T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822941 | ||||||
chr9:37822964
|
C | T | 1 | a0001c0001t0061g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653+3563C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822964 | ||||||
chr9:37823248
|
A | G | 2 | a0001c0001t0002g0266a0001c0001t0002g0273 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.653+3847A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823248 | ||||||
chr9:37823540
|
T | C | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+4139T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823540 | ||||||
chr9:37823586
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+4185G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823586 | ||||||
chr9:37823589
|
G | GT | 39 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(36): Show | 40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.653+4195dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823589 | |||||
chr9:37823596
|
T | TTG | 13 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(10): Show | 14 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.653+4195_653+4196i others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823596 | ||||||
chr9:37823599
|
C | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+4198C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823599 | ||||||
chr9:37823600
|
G | A | 1 | a0001c0001t0003g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.653+4199G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823600 | ||||||
chr9:37823699
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.653+4298T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823699 | ||||||
chr9:37823876
|
C | CT | 19 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0002g0280others(16): Show | 19 | HG00733.hp1 HG01978.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.653+4497dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823876 | |||||
chr9:37823876
|
CT | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0063a0001c0001t0001g0207others(17): Show | 22 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.653+4497delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823876 | |||||
chr9:37823919
|
TGCCCAGG others(15): Show |
T | 1 | a0001c0001t0005g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+4520_653+4541d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823919 | |||||
chr9:37824062
|
G | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+4661G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824062 | ||||||
chr9:37824083
|
G | A | 12 | a0001c0001t0016g0159a0001c0001t0016g0160a0001c0001t0016g0176others(9): Show | 13 | HG00741.hp1 HG01106.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.653+4682G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824083 | ||||||
chr9:37824170
|
C | T | 1 | a0001c0001t0020g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653+4769C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824170 | ||||||
chr9:37824182
|
T | C | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+4781T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824182 | ||||||
chr9:37824306
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+4905G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824306 | ||||||
chr9:37824320
|
A | C | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+4919A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824320 | ||||||
chr9:37824420
|
T | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+5019T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824420 | ||||||
chr9:37824508
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.653+5107A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824508 | ||||||
chr9:37824554
|
TA | T | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+5165delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37824554 | |||||
chr9:37824723
|
T | C | 347 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(344): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.653+5322T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824723 | ||||||
chr9:37824728
|
T | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+5327T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824728 | ||||||
chr9:37824939
|
A | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+5538A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824939 | ||||||
chr9:37825014
|
C | A | 1 | a0001c0001t0002g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.653+5613C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825014 | ||||||
chr9:37825036
|
T | C | 1 | a0001c0001t0002g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.653+5635T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825036 | ||||||
chr9:37825179
|
G | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5778G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825179 | ||||||
chr9:37825181
|
G | A | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5780G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825181 | ||||||
chr9:37825190
|
T | A | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5789T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825190 | ||||||
chr9:37825194
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5793A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825194 | ||||||
chr9:37825197
|
C | G | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5796C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825197 | ||||||
chr9:37825200
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5799A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825200 | ||||||
chr9:37825203
|
A | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5802A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825203 | ||||||
chr9:37825204
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5803A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825204 | ||||||
chr9:37825205
|
C | A | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5804C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825205 | ||||||
chr9:37825207
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5806A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825207 | ||||||
chr9:37825208
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5807C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825208 | ||||||
chr9:37825213
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5812A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825213 | ||||||
chr9:37825214
|
T | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5813T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825214 | ||||||
chr9:37825221
|
C | A | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5820C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825221 | ||||||
chr9:37825228
|
C | T | 2 | a0001c0001t0005g0018a0001c0001t0009g0017 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.653+5827C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825228 | ||||||
chr9:37825232
|
T | G | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5831T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825232 | ||||||
chr9:37825235
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5834C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825235 | ||||||
chr9:37825238
|
G | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5837G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825238 | ||||||
chr9:37825241
|
A | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5840A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825241 | ||||||
chr9:37825243
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5842A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825243 | ||||||
chr9:37825245
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5844A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825245 | ||||||
chr9:37825246
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5845C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825246 | ||||||
chr9:37825249
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5848A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825249 | ||||||
chr9:37825250
|
A | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5849A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825250 | ||||||
chr9:37825251
|
A | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5850A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825251 | ||||||
chr9:37825257
|
A | C | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5856A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825257 | ||||||
chr9:37825280
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5879C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825280 | ||||||
chr9:37825281
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5880A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825281 | ||||||
chr9:37825344
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.653+5943T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825344 | ||||||
chr9:37825565
|
C | T | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.653+6164C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825565 | ||||||
chr9:37825705
|
A | G | 2 | a0001c0001t0014g0088a0001c0001t0014g0202 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.653+6304A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825705 | ||||||
chr9:37825860
|
A | G | 1 | a0001c0001t0004g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.653+6459A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825860 | ||||||
chr9:37825903
|
C | T | 1 | a0001c0001t0015g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.653+6502C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825903 | ||||||
chr9:37825904
|
G | A | 1 | a0001c0001t0026g0006 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.653+6503G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825904 | ||||||
chr9:37825912
|
G | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(26): Show | 31 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.653+6511G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825912 | ||||||
chr9:37825913
|
T | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.653+6512T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825913 | ||||||
chr9:37825928
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+6527A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825928 | ||||||
chr9:37825992
|
G | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+6591G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825992 | ||||||
chr9:37826003
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.653+6602C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826003 | ||||||
chr9:37826014
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+6613G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826014 | ||||||
chr9:37826039
|
GA | G | 47 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(44): Show | 48 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+6650delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826039 | |||||
chr9:37826051
|
A | G | 1 | a0001c0001t0005g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+6650A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826051 | ||||||
chr9:37826052
|
G | T | 1 | a0001c0001t0005g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+6651G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826052 | ||||||
chr9:37826055
|
T | A | 1 | a0001c0001t0005g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+6654T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826055 | ||||||
chr9:37826076
|
T | TA | 15 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.653+6687dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826076 | |||||
chr9:37826076
|
TA | T | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+6687delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826076 | |||||
chr9:37826221
|
T | C | 4 | a0001c0001t0003g0004a0001c0001t0003g0171a0001c0001t0003g0185others(1): Show | 5 | HG01928.hp1 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+6820T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826221 | ||||||
chr9:37826288
|
G | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+6887G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826288 | ||||||
chr9:37826294
|
A | G | 1 | a0001c0001t0036g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.653+6893A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826294 | ||||||
chr9:37826422
|
A | G | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+7021A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826422 | ||||||
chr9:37826580
|
C | T | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+7179C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826580 | ||||||
chr9:37826614
|
C | T | 6 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+7213C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826614 | ||||||
chr9:37826820
|
C | CT | 11 | a0001c0001t0001g0067a0001c0001t0001g0078a0001c0001t0001g0098others(8): Show | 11 | HG02135.hp1 HG02135.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+7441dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | |||||
chr9:37826820
|
CTT | C | 38 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(35): Show | 38 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.653+7440_653+7441d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | |||||
chr9:37826820
|
CTTT | C | 5 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(2): Show | 6 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+7439_653+7441d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | |||||
chr9:37826820
|
CTTTT | C | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+7438_653+7441d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | |||||
chr9:37826878
|
A | T | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+7477A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826878 | ||||||
chr9:37826895
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.653+7494G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826895 | ||||||
chr9:37827240
|
T | C | 2 | a0001c0001t0001g0227a0001c0001t0023g0089 | 2 | HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.653+7839T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37827240 | ||||||
chr9:37827320
|
A | G | 2 | a0001c0001t0003g0185a0001c0001t0003g0190 | 2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.653+7919A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37827320 | ||||||
chr9:37827771
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.653+8370G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37827771 | ||||||
chr9:37827886
|
C | CTTATT | 4 | a0001c0001t0004g0086a0001c0001t0014g0201a0001c0001t0018g0341others(1): Show | 4 | HG02976.hp2 NA19043.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+8499_653+8503d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37827886 | |||||
chr9:37827886
|
C | CTTATTTT others(3): Show |
1 | a0001c0001t0014g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.653+8494_653+8503d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37827886 | |||||
chr9:37828223
|
G | A | 51 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(48): Show | 53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.653+8822G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828223 | ||||||
chr9:37828327
|
ACAAATAT others(35): Show |
A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00733.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.653+8928_653+8969d others(44): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37828327 | |||||
chr9:37828452
|
G | GA | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+9057dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37828452 | |||||
chr9:37828458
|
AG | A | 6 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+9058delG | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828458 | ||||||
chr9:37828459
|
G | A | 47 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(44): Show | 49 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.653+9058G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828459 | ||||||
chr9:37828758
|
C | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+9357C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828758 | ||||||
chr9:37829221
|
C | G | 1 | a0001c0001t0005g0024 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.653+9820C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829221 | ||||||
chr9:37829231
|
G | C | 1 | a0001c0001t0004g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.653+9830G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829231 | ||||||
chr9:37829266
|
C | T | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.653+9865C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829266 | ||||||
chr9:37829269
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+9868G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829269 | ||||||
chr9:37829296
|
C | T | 1 | a0001c0001t0007g0265 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.653+9895C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829296 | ||||||
chr9:37829306
|
C | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+9905C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829306 | ||||||
chr9:37829365
|
G | A | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+9964G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829365 | ||||||
chr9:37829368
|
A | G | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.653+9967A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829368 | ||||||
chr9:37829380
|
C | T | 1 | a0001c0001t0003g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.653+9979C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829380 | ||||||
chr9:37829582
|
C | G | 347 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(344): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.653+10181C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829582 | ||||||
chr9:37829603
|
C | T | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+10202C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829603 | ||||||
chr9:37829734
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.653+10333T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829734 | ||||||
chr9:37829740
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+10339C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829740 | ||||||
chr9:37829796
|
C | G | 3 | a0001c0001t0004g0140a0001c0001t0004g0172a0001c0001t0004g0196 | 3 | HG00597.hp2 NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.653+10395C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829796 | ||||||
chr9:37829807
|
G | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+10406G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829807 | ||||||
chr9:37829889
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+10488C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829889 | ||||||
chr9:37829949
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0210 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.653+10548G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829949 | ||||||
chr9:37830091
|
TAGAG | T | 53 | a0001c0001t0002g0272a0001c0001t0002g0275a0001c0001t0002g0294others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+10694_653+1069 others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37830091 | |||||
chr9:37830143
|
T | G | 5 | a0001c0001t0004g0142a0001c0001t0023g0177a0001c0002t0004g0178others(2): Show | 5 | HG01109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+10742T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830143 | ||||||
chr9:37830213
|
T | A | 5 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(2): Show | 5 | HG02451.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+10812T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830213 | ||||||
chr9:37830554
|
C | T | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+11153C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830554 | ||||||
chr9:37830636
|
G | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+11235G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830636 | ||||||
chr9:37831095
|
C | T | 5 | a0001c0001t0002g0272a0001c0001t0002g0275a0001c0001t0002g0294others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-10994C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831095 | ||||||
chr9:37831101
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.654-10988C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831101 | ||||||
chr9:37831131
|
C | T | 54 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(51): Show | 56 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.654-10958C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831131 | ||||||
chr9:37831215
|
TC | T | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-10873delC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831215 | ||||||
chr9:37831216
|
C | CA | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.654-10864dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37831216 | |||||
chr9:37831241
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-10848A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831241 | ||||||
chr9:37831365
|
T | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-10724T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831365 | ||||||
chr9:37831366
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-10723C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831366 | ||||||
chr9:37831559
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.654-10530G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831559 | ||||||
chr9:37831727
|
T | C | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.654-10362T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831727 | ||||||
chr9:37831823
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-10266T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831823 | ||||||
chr9:37832023
|
A | G | 347 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(344): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.654-10066A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832023 | ||||||
chr9:37832108
|
C | G | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-9981C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832108 | ||||||
chr9:37832150
|
A | T | 1 | a0001c0001t0001g0261 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.654-9939A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832150 | ||||||
chr9:37832150
|
AAAT | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(84): Show | 90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.654-9929_654-9927d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37832150 | |||||
chr9:37832153
|
T | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-9936T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832153 | ||||||
chr9:37832195
|
T | C | 18 | a0001c0001t0003g0092a0001c0001t0003g0134a0001c0001t0003g0137others(15): Show | 18 | HG00621.hp1 HG01192.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.654-9894T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832195 | ||||||
chr9:37832223
|
C | T | 4 | a0001c0001t0020g0048a0001c0001t0020g0049a0001c0001t0021g0001others(1): Show | 5 | HG01243.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-9866C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832223 | ||||||
chr9:37832233
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-9856G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832233 | ||||||
chr9:37832261
|
C | T | 1 | a0001c0001t0009g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.654-9828C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832261 | ||||||
chr9:37832303
|
C | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-9786C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832303 | ||||||
chr9:37832327
|
G | A | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.654-9762G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832327 | ||||||
chr9:37832415
|
G | A | 18 | a0001c0001t0002g0277a0001c0001t0002g0280a0001c0001t0002g0282others(15): Show | 18 | HG01516.hp1 HG01978.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.654-9674G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832415 | ||||||
chr9:37832458
|
C | CA | 11 | a0001c0001t0018g0341a0001c0001t0018g0342a0001c0001t0019g0051others(8): Show | 12 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.654-9616dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37832458 | |||||
chr9:37832789
|
C | T | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-9300C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832789 | ||||||
chr9:37832872
|
T | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.654-9217T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832872 | ||||||
chr9:37832879
|
TTTTTTG | T | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-9192_654-9187d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37832879 | |||||
chr9:37832957
|
T | C | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-9132T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832957 | ||||||
chr9:37833069
|
T | A | 1 | a0001c0001t0004g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.654-9020T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833069 | ||||||
chr9:37833298
|
C | T | 1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654-8791C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833298 | ||||||
chr9:37833784
|
A | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-8305A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833784 | ||||||
chr9:37833815
|
C | T | 1 | a0001c0001t0040g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.654-8274C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833815 | ||||||
chr9:37833844
|
G | C | 2 | a0001c0001t0019g0051a0001c0001t0019g0052 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.654-8245G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833844 | ||||||
chr9:37834053
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0033g0053 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.654-8036C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834053 | ||||||
chr9:37834058
|
G | C | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-8031G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834058 | ||||||
chr9:37834098
|
C | T | 1 | a0001c0001t0014g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.654-7991C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834098 | ||||||
chr9:37834165
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-7924T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834165 | ||||||
chr9:37834214
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-7875G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834214 | ||||||
chr9:37834373
|
C | T | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-7716C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834373 | ||||||
chr9:37834444
|
A | G | 1 | a0001c0001t0004g0175 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.654-7645A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834444 | ||||||
chr9:37834664
|
C | T | 347 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(344): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.654-7425C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834664 | ||||||
chr9:37834790
|
C | T | 1 | a0001c0001t0003g0183 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.654-7299C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834790 | ||||||
chr9:37834794
|
C | CTTTTTTT others(1): Show |
39 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(36): Show | 40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.654-7291_654-7284d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37834794 | |||||
chr9:37834794
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(3): Show | 7 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.654-7292_654-7284d others(11): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37834794 | |||||
chr9:37834794
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(5): Show | 8 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.654-7293_654-7284d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37834794 | |||||
chr9:37834891
|
A | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-7198A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834891 | ||||||
chr9:37835156
|
C | T | 1 | a0001c0001t0003g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.654-6933C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835156 | ||||||
chr9:37835303
|
G | A | 5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0024g0215others(2): Show | 5 | HG00140.hp1 HG01074.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.654-6786G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835303 | ||||||
chr9:37835352
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.654-6737G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835352 | ||||||
chr9:37835382
|
C | T | 64 | a0001c0001t0001g0281a0001c0001t0002g0060a0001c0001t0002g0091others(61): Show | 64 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.654-6707C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835382 | ||||||
chr9:37835533
|
G | A | 1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654-6556G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835533 | ||||||
chr9:37835567
|
G | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.654-6522G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835567 | ||||||
chr9:37835691
|
G | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-6398G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835691 | ||||||
chr9:37836101
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-5988G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836101 | ||||||
chr9:37836262
|
G | T | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-5827G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836262 | ||||||
chr9:37836511
|
T | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-5578T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836511 | ||||||
chr9:37836629
|
GA | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-5459delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836629 | ||||||
chr9:37836716
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.654-5373T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836716 | ||||||
chr9:37836944
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-5145T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836944 | ||||||
chr9:37837044
|
G | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-5045G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837044 | ||||||
chr9:37837102
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.654-4987A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837102 | ||||||
chr9:37837143
|
C | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4946C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837143 | ||||||
chr9:37837328
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4761A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837328 | ||||||
chr9:37837415
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-4674C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837415 | ||||||
chr9:37837433
|
T | G | 1 | a0001c0001t0034g0339 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.654-4656T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837433 | ||||||
chr9:37837450
|
T | C | 1 | a0001c0001t0004g0343 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.654-4639T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837450 | ||||||
chr9:37837453
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4636A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837453 | ||||||
chr9:37837457
|
C | CA | 9 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0109others(6): Show | 9 | HG00621.hp2 HG01981.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.654-4614dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837457 | |||||
chr9:37837457
|
CAAAA | C | 51 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(48): Show | 53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.654-4617_654-4614d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837457 | |||||
chr9:37837472
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.654-4617A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837472 | ||||||
chr9:37837520
|
A | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4569A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837520 | ||||||
chr9:37837650
|
G | T | 50 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(47): Show | 52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.654-4439G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837650 | ||||||
chr9:37837845
|
C | CA | 35 | a0001c0001t0001g0096a0001c0001t0001g0152a0001c0001t0001g0153others(32): Show | 35 | HG00558.hp2 HG01081.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.654-4230dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837845 | |||||
chr9:37837845
|
C | CAA | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-4231_654-4230d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837845 | |||||
chr9:37837845
|
C | CAAA | 10 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(7): Show | 10 | HG01496.hp2 HG02451.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.654-4232_654-4230d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837845 | |||||
chr9:37838063
|
A | G | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654-4026A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37838063 | ||||||
chr9:37838071
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.654-4018T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37838071 | ||||||
chr9:37838438
|
T | TA | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-3644dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37838438 | |||||
chr9:37839018
|
C | CAGAAATT others(5): Show |
1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-3070_654-3069i others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839018 | |||||
chr9:37839020
|
T | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-3069T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839020 | ||||||
chr9:37839021
|
C | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-3068C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839021 | ||||||
chr9:37839048
|
A | AT | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-3031dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839048 | |||||
chr9:37839065
|
C | CT | 22 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(19): Show | 24 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.654-3016dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839065 | |||||
chr9:37839065
|
C | CTT | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.654-3017_654-3016d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839065 | |||||
chr9:37839148
|
G | A | 1 | a0001c0001t0055g0264 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.654-2941G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839148 | ||||||
chr9:37839247
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.654-2842A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839247 | ||||||
chr9:37839347
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.654-2742A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839347 | ||||||
chr9:37839359
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0241a0001c0001t0001g0243 | 3 | NA18959.hp1 NA19062.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.654-2730C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839359 | ||||||
chr9:37839529
|
C | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0066others(21): Show | 25 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.654-2560C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839529 | ||||||
chr9:37839531
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.654-2558C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839531 | ||||||
chr9:37839795
|
C | T | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-2294C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839795 | ||||||
chr9:37839822
|
C | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-2267C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839822 | ||||||
chr9:37839875
|
G | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-2214G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839875 | ||||||
chr9:37839949
|
C | T | 1 | a0001c0001t0015g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.654-2140C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839949 | ||||||
chr9:37840024
|
C | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-2065C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840024 | ||||||
chr9:37840161
|
A | C | 1 | a0001c0001t0002g0312 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.654-1928A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840161 | ||||||
chr9:37840294
|
G | C | 1 | a0001c0001t0001g0330 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.654-1795G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840294 | ||||||
chr9:37840364
|
C | G | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-1725C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840364 | ||||||
chr9:37840446
|
T | A | 1 | a0001c0001t0016g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.654-1643T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840446 | ||||||
chr9:37840539
|
T | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-1550T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840539 | ||||||
chr9:37840555
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.654-1534C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840555 | ||||||
chr9:37840616
|
C | T | 6 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.654-1473C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840616 | ||||||
chr9:37840670
|
T | A | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-1419T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840670 | ||||||
chr9:37840690
|
A | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-1399A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840690 | ||||||
chr9:37840892
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0017g0076 | 2 | HG02071.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.654-1197A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840892 | ||||||
chr9:37840898
|
ATACT | A | 3 | a0001c0001t0001g0094a0001c0001t0013g0056a0001c0001t0013g0057 | 3 | HG00733.hp2 HG01255.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.654-1187_654-1184d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37840898 | |||||
chr9:37840905
|
C | T | 4 | a0001c0001t0002g0280a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | NA18994.hp2 NA19062.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-1184C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840905 | ||||||
chr9:37840912
|
G | T | 1 | a0001c0001t0001g0009 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.654-1177G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840912 | ||||||
chr9:37840953
|
C | A | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-1136C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840953 | ||||||
chr9:37840991
|
T | C | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-1098T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840991 | ||||||
chr9:37841166
|
G | A | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0006g0253others(5): Show | 8 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-923G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841166 | ||||||
chr9:37841176
|
C | G | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0087others(105): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.654-913C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841176 | ||||||
chr9:37841201
|
G | A | 7 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-888G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841201 | ||||||
chr9:37841251
|
T | C | 42 | a0001c0001t0003g0004a0001c0001t0003g0083a0001c0001t0003g0084others(39): Show | 43 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.654-838T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841251 | ||||||
chr9:37841383
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-706A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841383 | ||||||
chr9:37841585
|
A | C | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654-504A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841585 | ||||||
chr9:37842340
|
G | C | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+54G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842340 | ||||||
chr9:37842611
|
T | C | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+325T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842611 | ||||||
chr9:37842719
|
G | A | 4 | a0001c0001t0009g0013a0001c0001t0009g0033a0001c0001t0027g0014others(1): Show | 4 | NA18957.hp1 NA18960.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+433G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842719 | ||||||
chr9:37842975
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.851+689T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842975 | ||||||
chr9:37842994
|
C | A | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.851+708C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842994 | ||||||
chr9:37843049
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.851+763G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843049 | ||||||
chr9:37843099
|
A | T | 1 | a0001c0001t0062g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.851+813A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843099 | ||||||
chr9:37843268
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.851+982T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843268 | ||||||
chr9:37843324
|
C | T | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+1038C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843324 | ||||||
chr9:37843362
|
G | A | 2 | a0001c0001t0004g0239a0001c0001t0053g0240 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.851+1076G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843362 | ||||||
chr9:37843432
|
G | C | 6 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+1146G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843432 | ||||||
chr9:37843688
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851+1402T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843688 | ||||||
chr9:37844032
|
C | T | 1 | a0001c0001t0006g0259 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.851+1746C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844032 | ||||||
chr9:37844242
|
C | T | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0006g0253others(5): Show | 8 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.851+1956C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844242 | ||||||
chr9:37844243
|
G | A | 39 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(36): Show | 39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.851+1957G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844243 | ||||||
chr9:37844293
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.851+2007G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844293 | ||||||
chr9:37844374
|
C | T | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+2088C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844374 | ||||||
chr9:37844398
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.851+2112C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844398 | ||||||
chr9:37844471
|
A | G | 242 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0087others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.851+2185A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844471 | ||||||
chr9:37844533
|
C | A | 1 | a0001c0001t0002g0315 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.851+2247C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844533 | ||||||
chr9:37844592
|
C | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.851+2306C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844592 | ||||||
chr9:37844605
|
T | C | 1 | a0001c0001t0021g0001 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.851+2319T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844605 | ||||||
chr9:37844699
|
G | T | 1 | a0001c0001t0021g0001 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.851+2413G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844699 | ||||||
chr9:37844750
|
C | T | 43 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(40): Show | 45 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.851+2464C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844750 | ||||||
chr9:37844827
|
TAAC | T | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+2553_851+2555d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37844827 | |||||
chr9:37844856
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.851+2570G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844856 | ||||||
chr9:37844904
|
AT | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+2621delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37844904 | |||||
chr9:37845332
|
G | A | 1 | a0001c0001t0041g0228 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.851+3046G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845332 | ||||||
chr9:37845560
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.851+3274A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845560 | ||||||
chr9:37845706
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.851+3420A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845706 | ||||||
chr9:37845743
|
C | T | 1 | a0001c0001t0004g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.851+3457C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845743 | ||||||
chr9:37845803
|
T | G | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+3517T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845803 | ||||||
chr9:37845965
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+3679A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845965 | ||||||
chr9:37846353
|
A | G | 1 | a0001c0001t0015g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.851+4067A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846353 | ||||||
chr9:37846398
|
C | T | 3 | a0001c0001t0002g0294a0001c0001t0002g0306a0001c0001t0007g0293 | 3 | HG01891.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.851+4112C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846398 | ||||||
chr9:37846412
|
G | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.851+4126G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846412 | ||||||
chr9:37846489
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+4203G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846489 | ||||||
chr9:37846691
|
A | G | 80 | a0001c0001t0001g0281a0001c0001t0002g0060a0001c0001t0002g0091others(77): Show | 80 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.851+4405A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846691 | ||||||
chr9:37846703
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+4417A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846703 | ||||||
chr9:37846724
|
G | A | 6 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+4438G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846724 | ||||||
chr9:37846920
|
C | T | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+4634C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846920 | ||||||
chr9:37846924
|
T | C | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+4638T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846924 | ||||||
chr9:37847024
|
C | T | 8 | a0001c0001t0002g0060a0001c0001t0002g0321a0001c0001t0008g0041others(5): Show | 8 | HG02080.hp1 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.851+4738C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847024 | ||||||
chr9:37847146
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+4860A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847146 | ||||||
chr9:37847213
|
A | G | 1 | a0001c0001t0002g0311 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.851+4927A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847213 | ||||||
chr9:37847226
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.851+4940C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847226 | ||||||
chr9:37847253
|
C | CA | 12 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0105others(9): Show | 12 | HG00323.hp2 HG00735.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.851+4991dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | |||||
chr9:37847253
|
CA | C | 17 | a0001c0001t0001g0127a0001c0001t0001g0153a0001c0001t0001g0204others(14): Show | 17 | HG00140.hp1 HG01069.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.851+4991delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | |||||
chr9:37847253
|
CAA | C | 33 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(30): Show | 33 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.851+4990_851+4991d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | |||||
chr9:37847253
|
CAAAA | C | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.851+4988_851+4991d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | |||||
chr9:37847253
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.851+4982_851+4991d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | |||||
chr9:37847253
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0004g0142a0001c0002t0004g0178a0001c0002t0004g0179others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+4980_851+4991d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | |||||
chr9:37847296
|
T | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+5010T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847296 | ||||||
chr9:37847300
|
TA | T | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+5025delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847300 | |||||
chr9:37847322
|
A | G | 8 | a0001c0001t0001g0281a0001c0001t0007g0265a0001c0001t0007g0268others(5): Show | 8 | NA18947.hp1 NA18952.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.851+5036A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847322 | ||||||
chr9:37847330
|
C | A | 8 | a0001c0001t0001g0281a0001c0001t0007g0265a0001c0001t0007g0268others(5): Show | 8 | NA18947.hp1 NA18952.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.851+5044C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847330 | ||||||
chr9:37848037
|
G | T | 1 | a0001c0001t0003g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.851+5751G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848037 | ||||||
chr9:37848256
|
CA | C | 4 | a0001c0001t0011g0232a0001c0001t0011g0233a0001c0001t0011g0234others(1): Show | 4 | NA18955.hp1 NA18979.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+5973delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848256 | |||||
chr9:37848282
|
G | T | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+5996G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848282 | ||||||
chr9:37848352
|
G | A | 1 | a0001c0001t0009g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.851+6066G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848352 | ||||||
chr9:37848378
|
A | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+6092A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848378 | ||||||
chr9:37848413
|
G | A | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+6127G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848413 | ||||||
chr9:37848486
|
C | T | 7 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+6200C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848486 | ||||||
chr9:37848526
|
T | C | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+6240T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848526 | ||||||
chr9:37848572
|
A | G | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.852-6208A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848572 | ||||||
chr9:37848602
|
A | C | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-6178A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848602 | ||||||
chr9:37848626
|
C | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0126 | 2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.852-6154C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848626 | ||||||
chr9:37848635
|
G | A | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-6145G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848635 | ||||||
chr9:37848737
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.852-6043C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848737 | ||||||
chr9:37848741
|
G | T | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-6039G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848741 | ||||||
chr9:37848742
|
GA | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-6037delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848742 | ||||||
chr9:37848798
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-5982T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848798 | ||||||
chr9:37848967
|
T | C | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-5813T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848967 | ||||||
chr9:37848972
|
C | CA | 12 | a0001c0001t0001g0208a0001c0001t0002g0267a0001c0001t0003g0197others(9): Show | 12 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.852-5789dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848972 | |||||
chr9:37848972
|
CAA | C | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-5790_852-5789d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848972 | |||||
chr9:37848972
|
CAAA | C | 39 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(36): Show | 39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.852-5791_852-5789d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848972 | |||||
chr9:37848989
|
A | C | 1 | a0001c0001t0001g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.852-5791A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848989 | ||||||
chr9:37849247
|
A | G | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.852-5533A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849247 | ||||||
chr9:37849441
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852-5339A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849441 | ||||||
chr9:37849476
|
C | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-5304C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849476 | ||||||
chr9:37849512
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.852-5268C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849512 | ||||||
chr9:37849603
|
C | T | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.852-5177C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849603 | ||||||
chr9:37849610
|
C | G | 1 | a0001c0001t0004g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.852-5170C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849610 | ||||||
chr9:37849835
|
G | A | 39 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(36): Show | 39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.852-4945G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849835 | ||||||
chr9:37849847
|
T | A | 1 | a0001c0001t0032g0050 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.852-4933T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849847 | ||||||
chr9:37849894
|
C | A | 2 | a0001c0001t0004g0239a0001c0001t0053g0240 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.852-4886C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849894 | ||||||
chr9:37849897
|
A | C | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-4883A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849897 | ||||||
chr9:37849925
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0013g0056a0001c0001t0013g0057others(2): Show | 5 | HG00733.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.852-4855C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849925 | ||||||
chr9:37849949
|
C | T | 1 | a0001c0001t0016g0176 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.852-4831C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849949 | ||||||
chr9:37849960
|
G | A | 4 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-4820G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849960 | ||||||
chr9:37849984
|
A | T | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-4796A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849984 | ||||||
chr9:37850082
|
GGGCCAAA others(11): Show |
G | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-4690_852-4673d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850082 | |||||
chr9:37850128
|
T | C | 1 | a0001c0001t0010g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.852-4652T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850128 | ||||||
chr9:37850253
|
T | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-4527T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850253 | ||||||
chr9:37850312
|
A | G | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-4468A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850312 | ||||||
chr9:37850475
|
G | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-4305G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850475 | ||||||
chr9:37850736
|
A | G | 3 | a0001c0001t0004g0140a0001c0001t0004g0172a0001c0001t0004g0196 | 3 | HG00597.hp2 NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.852-4044A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850736 | ||||||
chr9:37850818
|
GATATATT others(6): Show |
G | 1 | a0001c0001t0003g0163 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.852-3955_852-3943d others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850818 | |||||
chr9:37850820
|
T | C | 2 | a0001c0001t0017g0327a0001c0001t0017g0328 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.852-3960T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850820 | ||||||
chr9:37850823
|
A | T | 1 | a0001c0001t0003g0195 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.852-3957A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850823 | ||||||
chr9:37850825
|
T | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-3955T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850825 | ||||||
chr9:37850825
|
TTTATATA others(4): Show |
T | 1 | a0001c0001t0003g0195 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.852-3953_852-3943d others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850825 | |||||
chr9:37850826
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0007g0293 | 2 | HG00558.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.852-3954T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850826 | ||||||
chr9:37850826
|
T | TTA | 24 | a0001c0001t0001g0065a0001c0001t0001g0109a0001c0001t0001g0117others(21): Show | 24 | HG00733.hp1 HG01261.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.852-3899_852-3898d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATA | 21 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0071others(18): Show | 22 | HG01978.hp2 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.852-3901_852-3898d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATA | 11 | a0001c0001t0001g0125a0001c0001t0001g0337a0001c0001t0001g0338others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.852-3903_852-3898d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATAT others(1): Show |
8 | a0001c0001t0001g0127a0001c0001t0001g0246a0001c0001t0001g0247others(5): Show | 8 | HG01069.hp2 HG02080.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-3905_852-3898d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATAT others(3): Show |
10 | a0001c0001t0001g0063a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG02080.hp1 HG02897.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.852-3907_852-3898d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0121a0001c0001t0002g0311 | 2 | HG01928.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.852-3909_852-3898d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0006g0278 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.852-3913_852-3898d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0102a0001c0001t0002g0258 | 2 | HG01109.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.852-3915_852-3898d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0002g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.852-3919_852-3898d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTA | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0098a0001c0001t0001g0107others(25): Show | 29 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.852-3899_852-3898d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATA | T | 18 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0103others(15): Show | 18 | HG00558.hp1 HG01099.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.852-3901_852-3898d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATA | T | 14 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0090others(11): Show | 14 | HG00621.hp2 HG01978.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.852-3903_852-3898d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(1): Show |
T | 10 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0001g0111others(7): Show | 10 | HG01074.hp1 HG01123.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.852-3905_852-3898d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(3): Show |
T | 8 | a0001c0001t0002g0256a0001c0001t0005g0018a0001c0001t0008g0041others(5): Show | 8 | HG00140.hp1 HG02074.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.852-3907_852-3898d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(5): Show |
T | 14 | a0001c0001t0001g0208a0001c0001t0001g0242a0001c0001t0001g0330others(11): Show | 14 | HG00741.hp2 HG01975.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-3909_852-3898d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(7): Show |
T | 11 | a0001c0001t0001g0062a0001c0001t0003g0158a0001c0001t0005g0023others(8): Show | 11 | HG01192.hp1 HG01975.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.852-3911_852-3898d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(9): Show |
T | 10 | a0001c0001t0003g0197a0001c0001t0004g0086a0001c0001t0005g0020others(7): Show | 10 | HG00642.hp1 HG00741.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.852-3913_852-3898d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(11): Show |
T | 19 | a0001c0001t0001g0249a0001c0001t0003g0131a0001c0001t0003g0136others(16): Show | 19 | HG00621.hp1 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.852-3915_852-3898d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(13): Show |
T | 21 | a0001c0001t0001g0094a0001c0001t0001g0152a0001c0001t0001g0153others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.852-3917_852-3898d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(15): Show |
T | 40 | a0001c0001t0001g0093a0001c0001t0001g0168a0001c0001t0001g0174others(37): Show | 42 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.852-3919_852-3898d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(17): Show |
T | 9 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0150others(6): Show | 10 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.852-3921_852-3898d others(26): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(19): Show |
T | 3 | a0001c0001t0001g0116a0001c0001t0016g0176a0001c0001t0040g0199 | 3 | HG01515.hp2 HG06807.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.852-3923_852-3898d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(21): Show |
T | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.852-3925_852-3898d others(30): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0207 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.852-3927_852-3898d others(32): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(27): Show |
T | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-3931_852-3898d others(36): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850826
|
TTATATAT others(33): Show |
T | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-3937_852-3898d others(42): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | |||||
chr9:37850827
|
TATATATA others(14): Show |
T | 2 | a0001c0001t0003g0146a0001c0001t0003g0147 | 2 | NA18970.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.852-3952_852-3932d others(23): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850827 | ||||||
chr9:37850832
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0026g0006 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.852-3939_852-3938i others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850832 | |||||
chr9:37850834
|
A | T | 3 | a0001c0001t0003g0137a0001c0001t0003g0138a0001c0001t0003g0139 | 3 | NA18960.hp1 NA18980.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.852-3946A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850834 | ||||||
chr9:37850836
|
A | T | 2 | a0001c0001t0001g0214a0001c0001t0050g0217 | 2 | HG01074.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.852-3944A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850836 | ||||||
chr9:37850838
|
A | T | 2 | a0001c0001t0024g0215a0001c0001t0024g0216 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.852-3942A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850838 | ||||||
chr9:37850840
|
A | T | 1 | a0001c0001t0003g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.852-3940A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850840 | ||||||
chr9:37850842
|
A | G | 2 | a0001c0001t0011g0233a0001c0001t0044g0231 | 2 | HG03017.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.852-3938A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850842 | ||||||
chr9:37850842
|
A | T | 3 | a0001c0001t0003g0158a0001c0001t0014g0129a0001c0001t0043g0157 | 3 | HG01192.hp1 HG01975.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.852-3938A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850842 | ||||||
chr9:37850844
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0004g0007others(8): Show | 12 | HG00438.hp2 HG00735.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.852-3936A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850844 | ||||||
chr9:37850844
|
A | T | 1 | a0001c0001t0003g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.852-3936A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850844 | ||||||
chr9:37850846
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0048g0237 | 2 | HG01099.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.852-3934A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850846 | ||||||
chr9:37850846
|
A | T | 8 | a0001c0001t0001g0249a0001c0001t0003g0131a0001c0001t0003g0136others(5): Show | 8 | HG00621.hp1 HG01071.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-3934A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850846 | ||||||
chr9:37850848
|
A | T | 18 | a0001c0001t0001g0094a0001c0001t0001g0152a0001c0001t0001g0153others(15): Show | 18 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.852-3932A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850848 | ||||||
chr9:37850850
|
A | T | 35 | a0001c0001t0001g0093a0001c0001t0001g0168a0001c0001t0001g0174others(32): Show | 37 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.852-3930A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850850 | ||||||
chr9:37850852
|
A | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0003g0161others(2): Show | 6 | HG00323.hp2 HG01081.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-3928A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850852 | ||||||
chr9:37850854
|
A | T | 1 | a0001c0001t0040g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.852-3926A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850854 | ||||||
chr9:37850878
|
A | G | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-3902A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850878 | ||||||
chr9:37850881
|
T | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0236a0001c0001t0004g0007others(10): Show | 15 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-3899T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850881 | ||||||
chr9:37850881
|
T | TATATATA others(7): Show |
1 | a0001c0001t0002g0324 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.852-3898_852-3897i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850881 | |||||
chr9:37850882
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0006g0252 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.852-3898_852-3897i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850882 | ||||||
chr9:37851060
|
A | G | 1 | a0001c0001t0044g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852-3720A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851060 | ||||||
chr9:37851099
|
C | G | 5 | a0001c0001t0002g0272a0001c0001t0002g0275a0001c0001t0002g0294others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-3681C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851099 | ||||||
chr9:37851390
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-3390G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851390 | ||||||
chr9:37851421
|
C | T | 23 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(20): Show | 25 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.852-3359C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851421 | ||||||
chr9:37851433
|
G | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0337others(1): Show | 4 | HG01099.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-3347G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851433 | ||||||
chr9:37851553
|
G | C | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-3227G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851553 | ||||||
chr9:37851560
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.852-3220C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851560 | ||||||
chr9:37851668
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-3112G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851668 | ||||||
chr9:37851680
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-3100G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851680 | ||||||
chr9:37851688
|
G | A | 2 | a0001c0001t0002g0258a0001c0001t0006g0257 | 2 | HG01109.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.852-3092G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851688 | ||||||
chr9:37851693
|
G | GCTGAGGC others(12): Show |
1 | a0001c0001t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.852-3086_852-3068d others(21): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851693 | |||||
chr9:37851788
|
A | AAAAT | 3 | a0001c0001t0006g0253a0001c0001t0006g0254a0001c0001t0006g0255 | 3 | HG01361.hp2 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.852-2970_852-2967d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851788 | |||||
chr9:37851788
|
AAAAT | A | 6 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0001t0001g0188others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-2970_852-2967d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851788 | |||||
chr9:37851791
|
AT | A | 52 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(49): Show | 54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-2988delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851791 | ||||||
chr9:37851796
|
T | A | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.852-2984T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851796 | ||||||
chr9:37851810
|
A | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.852-2970A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851810 | ||||||
chr9:37851866
|
C | CCGAAA | 6 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(3): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-2914_852-2913i others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851866 | ||||||
chr9:37851866
|
C | CTGAAA | 47 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(44): Show | 48 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.852-2908_852-2904d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851866 | |||||
chr9:37852080
|
A | C | 1 | a0001c0001t0032g0050 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.852-2700A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852080 | ||||||
chr9:37852140
|
C | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-2640C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852140 | ||||||
chr9:37852602
|
A | AAG | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-2175_852-2174d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852602 | |||||
chr9:37852648
|
C | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG00621.hp2 HG02080.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.852-2132C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852648 | ||||||
chr9:37852681
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0015g0035 | 2 | HG00099.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.852-2099C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852681 | ||||||
chr9:37852682
|
G | A | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-2098G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852682 | ||||||
chr9:37852736
|
C | G | 10 | a0001c0001t0002g0091a0001c0001t0002g0263a0001c0001t0002g0270others(7): Show | 10 | HG00558.hp1 HG03239.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.852-2044C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852736 | ||||||
chr9:37852864
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.852-1916T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852864 | ||||||
chr9:37852930
|
T | TTA | 21 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0078others(18): Show | 21 | HG01099.hp2 HG01516.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.852-1815_852-1814d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATA | 22 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0077others(19): Show | 23 | HG00099.hp1 HG00621.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.852-1817_852-1814d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATA | 17 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(14): Show | 17 | HG00558.hp2 HG01261.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.852-1819_852-1814d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(1): Show |
25 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0105others(22): Show | 26 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.852-1821_852-1814d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(3): Show |
41 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0114others(38): Show | 41 | HG00741.hp2 HG01109.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.852-1823_852-1814d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(5): Show |
16 | a0001c0001t0001g0063a0001c0001t0001g0110a0001c0001t0001g0214others(13): Show | 16 | HG00642.hp2 HG01074.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.852-1825_852-1814d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(7): Show |
13 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0107others(10): Show | 13 | HG02132.hp2 HG02135.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.852-1827_852-1814d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG01257.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.852-1829_852-1814d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0002g0297 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.852-1831_852-1814d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0024g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.852-1833_852-1814d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTA | T | 7 | a0001c0001t0001g0281a0001c0001t0004g0218a0001c0001t0007g0265others(4): Show | 7 | HG03195.hp1 NA18947.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.852-1815_852-1814d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATA | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0205a0001c0001t0001g0236others(1): Show | 5 | HG03654.hp1 NA18986.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-1817_852-1814d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATATAT others(3): Show |
T | 2 | a0001c0001t0002g0282a0001c0001t0007g0288 | 2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.852-1823_852-1814d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0006g0260 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.852-1825_852-1814d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0103a0001c0001t0002g0314 | 2 | HG02055.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.852-1827_852-1814d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATATAT others(9): Show |
T | 3 | a0001c0001t0001g0128a0001c0001t0003g0083a0001c0001t0003g0084 | 3 | HG00099.hp2 HG00738.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.852-1829_852-1814d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATATAT others(11): Show |
T | 103 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(100): Show | 108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.852-1831_852-1814d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852930
|
TTATATAT others(13): Show |
T | 41 | a0001c0001t0001g0344a0001c0001t0005g0016a0001c0001t0005g0018others(38): Show | 41 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.852-1833_852-1814d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | |||||
chr9:37852950
|
A | T | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-1830A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852950 | ||||||
chr9:37852965
|
T | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-1815T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852965 | ||||||
chr9:37852965
|
T | TATATATA others(6): Show |
1 | a0001c0001t0002g0289 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.852-1814_852-1813i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852965 | |||||
chr9:37852966
|
A | ATATAT | 3 | a0001c0001t0001g0069a0001c0001t0002g0256a0001c0001t0042g0276 | 3 | HG02071.hp2 HG02074.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.852-1814_852-1813i others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852966 | ||||||
chr9:37852966
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0242 | 2 | HG02155.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.852-1814_852-1813i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852966 | ||||||
chr9:37853040
|
T | G | 27 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(24): Show | 27 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.852-1740T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853040 | ||||||
chr9:37853067
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-1713G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853067 | ||||||
chr9:37853108
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.852-1672C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853108 | ||||||
chr9:37853120
|
C | G | 1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.852-1660C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853120 | ||||||
chr9:37853144
|
C | T | 5 | a0001c0001t0014g0088a0001c0001t0014g0129a0001c0001t0014g0201others(2): Show | 5 | HG03209.hp2 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.852-1636C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853144 | ||||||
chr9:37853148
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.852-1632G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853148 | ||||||
chr9:37853152
|
C | CA | 12 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0001t0001g0222others(9): Show | 12 | HG01109.hp1 HG02055.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.852-1612dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | |||||
chr9:37853152
|
C | CAA | 31 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(28): Show | 31 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.852-1613_852-1612d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | |||||
chr9:37853152
|
C | CAAA | 8 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(5): Show | 8 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-1614_852-1612d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | |||||
chr9:37853152
|
C | CAAAA | 10 | a0001c0001t0008g0045a0001c0001t0012g0002a0001c0001t0012g0054others(7): Show | 12 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.852-1615_852-1612d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | |||||
chr9:37853284
|
G | A | 1 | a0001c0001t0051g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.852-1496G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853284 | ||||||
chr9:37853339
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-1441A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853339 | ||||||
chr9:37853356
|
CGAGCTGA | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-1421_852-1415d others(9): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853356 | |||||
chr9:37853366
|
C | G | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-1414C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853366 | ||||||
chr9:37853375
|
T | G | 1 | a0001c0001t0006g0278 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.852-1405T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853375 | ||||||
chr9:37853413
|
CA | C | 266 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0061others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.852-1348delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | |||||
chr9:37853413
|
CAA | C | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0344others(6): Show | 9 | HG01074.hp1 HG02738.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.852-1349_852-1348d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | |||||
chr9:37853413
|
CAAA | C | 37 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(34): Show | 37 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.852-1350_852-1348d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | |||||
chr9:37853413
|
CAAAA | C | 15 | a0001c0001t0008g0045a0001c0001t0012g0002a0001c0001t0012g0054others(12): Show | 17 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.852-1351_852-1348d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | |||||
chr9:37853443
|
T | C | 1 | a0001c0001t0010g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.852-1337T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853443 | ||||||
chr9:37853489
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.852-1291G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853489 | ||||||
chr9:37853503
|
C | CAAAAAGA others(274): Show |
1 | a0001c0001t0063g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.852-1261_852-1260i others(283): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853503 | |||||
chr9:37853511
|
T | C | 2 | a0001c0001t0004g0239a0001c0001t0053g0240 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.852-1269T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853511 | ||||||
chr9:37853548
|
T | G | 1 | a0001c0001t0006g0259 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.852-1232T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853548 | ||||||
chr9:37853649
|
CA | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-1130delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853649 | ||||||
chr9:37853651
|
G | T | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-1129G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853651 | ||||||
chr9:37853815
|
C | T | 40 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(37): Show | 40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.852-965C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853815 | ||||||
chr9:37853903
|
C | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0115a0001c0001t0001g0118others(1): Show | 4 | HG02129.hp2 NA18950.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-877C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853903 | ||||||
chr9:37854277
|
T | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-503T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854277 | ||||||
chr9:37854459
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.852-321A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854459 | ||||||
chr9:37854551
|
G | A | 1 | a0001c0001t0015g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.852-229G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854551 | ||||||
chr9:37854588
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.852-192A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854588 | ||||||
chr9:37855006
|
A | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1054+24A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855006 | ||||||
chr9:37855041
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1054+59G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855041 | ||||||
chr9:37855086
|
G | A | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1054+104G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855086 | ||||||
chr9:37855124
|
G | A | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1054+142G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855124 | ||||||
chr9:37855133
|
T | C | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1054+151T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855133 | ||||||
chr9:37855158
|
A | G | 1 | a0001c0001t0009g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1054+176A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855158 | ||||||
chr9:37855313
|
A | C | 1 | a0001c0001t0001g0241 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1054+331A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855313 | ||||||
chr9:37855389
|
G | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1054+407G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855389 | ||||||
chr9:37855536
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0004g0225others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+554C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855536 | ||||||
chr9:37855537
|
G | A | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+555G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855537 | ||||||
chr9:37855555
|
A | G | 31 | a0001c0001t0004g0086a0001c0001t0005g0016a0001c0001t0005g0018others(28): Show | 31 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054+573A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855555 | ||||||
chr9:37855699
|
G | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(87): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1054+717G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855699 | ||||||
chr9:37855700
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0093others(88): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1054+718C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855700 | ||||||
chr9:37855738
|
G | A | 4 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+756G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855738 | ||||||
chr9:37855750
|
C | T | 49 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0096others(46): Show | 49 | HG00558.hp2 HG00597.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1054+768C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855750 | ||||||
chr9:37855767
|
T | C | 1 | a0001c0001t0003g0147 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1054+785T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855767 | ||||||
chr9:37855827
|
C | A | 2 | a0001c0001t0045g0262a0001c0004t0047g0287 | 2 | HG02074.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1054+845C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855827 | ||||||
chr9:37855844
|
A | C | 1 | a0001c0001t0001g0330 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1054+862A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855844 | ||||||
chr9:37855991
|
A | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+1009A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855991 | ||||||
chr9:37856003
|
T | C | 3 | a0001c0001t0022g0345a0001c0001t0022g0346a0001c0001t0031g0347 | 3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1054+1021T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856003 | ||||||
chr9:37856183
|
A | T | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1055-1058A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856183 | ||||||
chr9:37856237
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0210 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1055-1004G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856237 | ||||||
chr9:37856471
|
G | GT | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1055-769dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 37856471 | |||||
chr9:37856514
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1055-727A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856514 | ||||||
chr9:37856636
|
TTA | T | 3 | a0001c0001t0003g0137a0001c0001t0003g0138a0001c0001t0003g0139 | 3 | NA18960.hp1 NA18980.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1055-603_1055-602d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 37856636 | |||||
chr9:37856685
|
C | T | 2 | a0001c0001t0006g0259a0001c0001t0006g0260 | 2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1055-556C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856685 | ||||||
chr9:37856783
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1055-458G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856783 | ||||||
chr9:37856787
|
C | CA | 12 | a0001c0001t0002g0289a0001c0001t0002g0291a0001c0001t0002g0297others(9): Show | 12 | HG02132.hp1 HG02148.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1055-445dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 37856787 | |||||
chr9:37857070
|
G | C | 13 | a0001c0001t0012g0002a0001c0001t0012g0054a0001c0001t0012g0055others(10): Show | 15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-171G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37857070 | ||||||
chr9:37857131
|
G | A | 1 | a0001c0001t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1055-110G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37857131 | ||||||
chr9:37857428
|
C | A | 2 | a0001c0001t0004g0239a0001c0001t0053g0240 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1165+77C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857428 | ||||||
chr9:37857606
|
G | A | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165+255G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857606 | ||||||
chr9:37857669
|
C | T | 9 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(6): Show | 10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165+318C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857669 | ||||||
chr9:37857681
|
GTATAAA | G | 4 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+336_1165+341d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 37857681 | |||||
chr9:37857708
|
G | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1165+357G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857708 | ||||||
chr9:37857964
|
G | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1165+613G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857964 | ||||||
chr9:37858037
|
C | CT | 17 | a0001c0001t0001g0168a0001c0001t0008g0041a0001c0001t0008g0042others(14): Show | 18 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.1165+696dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 37858037 | |||||
chr9:37858037
|
C | CTT | 7 | a0001c0001t0019g0051a0001c0001t0019g0052a0001c0001t0020g0048others(4): Show | 8 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+695_1165+696d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 37858037 | |||||
chr9:37858299
|
T | G | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1165+948T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858299 | ||||||
chr9:37858399
|
A | G | 29 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1165+1048A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858399 | ||||||
chr9:37858425
|
TG | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0210 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1165+1075delG | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858425 | ||||||
chr9:37858488
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1165+1137A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858488 | ||||||
chr9:37858655
|
G | T | 2 | a0001c0001t0018g0341a0001c0001t0018g0342 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1165+1304G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858655 | ||||||
chr9:37858864
|
C | G | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1166-1184C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858864 | ||||||
chr9:37858930
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1166-1118G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858930 | ||||||
chr9:37858963
|
C | T | 5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0024g0215others(2): Show | 5 | HG00140.hp1 HG01074.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-1085C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858963 | ||||||
chr9:37859124
|
T | C | 1 | a0001c0001t0001g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1166-924T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859124 | ||||||
chr9:37859149
|
G | C | 1 | a0001c0003t0030g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1166-899G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859149 | ||||||
chr9:37859397
|
C | A | 1 | a0003c0007t0008g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1166-651C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859397 | ||||||
chr9:37859734
|
G | A | 30 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(27): Show | 30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1166-314G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859734 | ||||||
chr9:37859883
|
C | T | 1 | a0001c0001t0058g0097 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1166-165C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859883 | ||||||
chr9:37859894
|
T | C | 9 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1166-154T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859894 | ||||||
chr9:37859953
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0002c0005t0001g0070 | 3 | NA18945.hp2 NA18957.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1166-95G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859953 | ||||||
chr9:37860208
|
A | G | 1 | a0001c0001t0016g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1311+15A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860208 | ||||||
chr9:37860230
|
T | C | 1 | a0001c0001t0040g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1311+37T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860230 | ||||||
chr9:37860261
|
G | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1311+68G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860261 | ||||||
chr9:37860269
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1311+76C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860269 | ||||||
chr9:37860377
|
C | A | 1 | a0001c0001t0014g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1311+184C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860377 | ||||||
chr9:37860395
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1311+202C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860395 | ||||||
chr9:37860492
|
T | TAAAC | 6 | a0001c0001t0001g0200a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+323_1311+326d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 37860492 | |||||
chr9:37860492
|
TAAAC | T | 27 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0023others(24): Show | 29 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1311+323_1311+326d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 37860492 | |||||
chr9:37860902
|
A | T | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0037g0187 | 3 | HG00099.hp2 HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1312-238A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860902 | ||||||
chr9:37860973
|
G | C | 53 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0020others(50): Show | 55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1312-167G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860973 |