Item | Value |
---|---|
geneid | 26094 |
ensemblid | ENSG00000119599.17 |
hgncid | 20229 |
symbol | DCAF4 |
name | DDB1 and CUL4 associated factor 4 |
refseq_nuc | NM_015604.4 |
refseq_prot | NP_056419.2 |
ensembl_nuc | ENST00000358377.7 |
ensembl_prot | ENSP00000351147.2 |
mane_status | MANE Select |
chr | chr14 |
start | 72926464 |
end | 72959703 |
strand | + |
ver | v1.2 |
region | chr14:72926464-72959703 |
region5000 | chr14:72921464-72964703 |
regionname0 | DCAF4_chr14_72926464_72959703 |
regionname5000 | DCAF4_chr14_72921464_72964703 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 495 | 329 | 78 | 59 | 147 | 8 | 36 | 113 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0002 | 0/0 | 495 | 44 | 4 | 7 | 31 | 0 | 2 | 25 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0003 | 0/0 | 495 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0004 | 0/0 | 495 | 6 | 0 | 2 | 2 | 1 | 1 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0005 | 0/0 | 495 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0006 | 0/0 | 495 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0007 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0008 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0009 | 0/1 | 495 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0010 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0011 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0012 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0013 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1488 | 193 | 49 | 43 | 80 | 3 | 17 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0002 | 0/0 | 1488 | 69 | 16 | 12 | 28 | 4 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0003 | 0/0 | 1488 | 59 | 8 | 4 | 37 | 1 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0004 | 0/0 | 1488 | 44 | 4 | 7 | 31 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0005 | 0/0 | 1488 | 6 | 0 | 0 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0006 | 0/0 | 1488 | 6 | 0 | 2 | 2 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0007 | 0/0 | 1488 | 5 | 5 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0008 | 0/0 | 1488 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0009 | 0/0 | 1488 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0010 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0011 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0012 | 0/1 | 1488 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0013 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0014 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0015 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0016 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0017 | 0/0 | 1488 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0018 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
c0019 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 987 | 104 | 24 | 17 | 41 | 6 | 14 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0002 | 0/0 | 987 | 95 | 2 | 20 | 63 | 2 | 8 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0003 | 0/0 | 987 | 55 | 2 | 5 | 37 | 1 | 10 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0004 | 0/0 | 987 | 42 | 37 | 5 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0005 | 0/0 | 987 | 28 | 2 | 13 | 6 | 1 | 6 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0006 | 0/0 | 987 | 27 | 4 | 4 | 19 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0007 | 0/0 | 987 | 18 | 1 | 3 | 12 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0008 | 0/0 | 987 | 13 | 12 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0009 | 0/0 | 987 | 8 | 1 | 1 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0010 | 0/0 | 987 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0011 | 0/0 | 987 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0012 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
t0013 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0360 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1488 | 193 | 49 | 43 | 80 | 3 | 17 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0001c0002 | 0/0 | 1488 | 69 | 16 | 12 | 28 | 4 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0001c0003 | 0/0 | 1488 | 59 | 8 | 4 | 37 | 1 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0001c0007 | 0/0 | 1488 | 5 | 5 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0001c0014 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0001c0015 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0001c0017 | 0/0 | 1488 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0002c0004 | 0/0 | 1488 | 44 | 4 | 7 | 31 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0003c0005 | 0/0 | 1488 | 6 | 0 | 0 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0004c0006 | 0/0 | 1488 | 6 | 0 | 2 | 2 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0005c0008 | 0/0 | 1488 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0006c0009 | 0/0 | 1488 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0007c0019 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0008c0010 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0009c0012 | 0/1 | 1488 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0010c0016 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0011c0011 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0012c0013 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 | |
a0013c0018 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2474 | 36 | 16 | 5 | 11 | 0 | 3 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0002 | 0/0 | 2474 | 88 | 2 | 20 | 56 | 2 | 8 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0003 | 0/0 | 2474 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0004 | 0/0 | 2474 | 27 | 24 | 3 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0005 | 0/0 | 2474 | 28 | 2 | 13 | 6 | 1 | 6 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0009 | 0/0 | 2474 | 8 | 1 | 1 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0010 | 0/0 | 2474 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0011 | 0/0 | 2474 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0001t0013 | 0/0 | 2474 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0002t0001 | 0/0 | 2474 | 56 | 5 | 10 | 28 | 4 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0002t0004 | 0/0 | 2474 | 13 | 11 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0003t0003 | 0/0 | 2474 | 52 | 2 | 4 | 36 | 1 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0003t0008 | 0/0 | 2474 | 7 | 6 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0007t0008 | 0/0 | 2474 | 5 | 5 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0014t0002 | 0/0 | 2474 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0015t0003 | 0/0 | 2474 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0001c0017t0003 | 0/0 | 2474 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0002c0004t0006 | 0/0 | 2474 | 26 | 3 | 4 | 19 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0002c0004t0007 | 0/0 | 2474 | 18 | 1 | 3 | 12 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0003c0005t0002 | 0/0 | 2474 | 6 | 0 | 0 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0004c0006t0001 | 0/0 | 2474 | 6 | 0 | 2 | 2 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0005c0008t0001 | 0/0 | 2474 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0006c0009t0001 | 0/0 | 2474 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0007c0019t0008 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0008c0010t0004 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0009c0012t0001 | 0/1 | 2474 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0010c0016t0006 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0011c0011t0004 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0012c0013t0012 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
a0013c0018t0001 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | copy fasta | chr14 | 72921464 | 72964703 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0009g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0001t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0002t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0003t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0007t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0007t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0007t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0007t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0007t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0014t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0015t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0001c0017t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0002c0004t0007g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0003c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0003c0005t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0003c0005t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0003c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0003c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0003c0005t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0004c0006t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0004c0006t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0004c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0004c0006t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0004c0006t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0005c0008t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0005c0008t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0006c0009t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0006c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0007c0019t0008g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0008c0010t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0009c0012t0001g0360 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0010c0016t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0011c0011t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0012c0013t0012g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
a0013c0018t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0338 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0348 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00140 | hp1 | a0001 | c0003 | t0003 | g0167 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00323 | hp1 | a0006 | c0009 | t0001 | g0194 | EUR | FIN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0363 | EUR | FIN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00423 | hp1 | a0002 | c0004 | t0006 | g0305 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00423 | hp2 | a0001 | c0003 | t0003 | g0179 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00639 | hp2 | a0001 | c0003 | t0003 | g0158 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00642 | hp1 | a0001 | c0003 | t0003 | g0013 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0369 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0353 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0368 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00735 | hp2 | a0002 | c0004 | t0007 | g0218 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00738 | hp1 | a0002 | c0004 | t0007 | g0114 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0243 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0373 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01069 | hp2 | a0002 | c0004 | t0006 | g0009 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0361 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0233 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01071 | hp2 | a0002 | c0004 | t0006 | g0009 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0260 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01167 | hp2 | a0001 | c0002 | t0004 | g0296 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0273 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01168 | hp2 | a0004 | c0006 | t0001 | g0011 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0358 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0281 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0326 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0354 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01261 | hp1 | a0004 | c0006 | t0001 | g0011 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01261 | hp2 | a0002 | c0004 | t0006 | g0307 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01346 | hp1 | a0001 | c0003 | t0003 | g0157 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0362 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01358 | hp2 | a0002 | c0004 | t0007 | g0222 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01433 | hp2 | a0001 | c0003 | t0003 | g0166 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01496 | hp1 | a0001 | c0002 | t0004 | g0376 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0229 | EUR | IBS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0277 | EUR | IBS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01891 | hp2 | a0001 | c0002 | t0004 | g0381 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0239 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0235 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02015 | hp2 | a0001 | c0015 | t0003 | g0172 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02027 | hp2 | a0002 | c0004 | t0006 | g0310 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0142 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02055 | hp1 | a0002 | c0004 | t0007 | g0220 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02074 | hp1 | a0001 | c0003 | t0003 | g0155 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02129 | hp2 | a0001 | c0003 | t0003 | g0113 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02135 | hp1 | a0002 | c0004 | t0006 | g0302 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02148 | hp2 | a0002 | c0004 | t0006 | g0297 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02155 | hp2 | a0001 | c0003 | t0003 | g0174 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02165 | hp1 | a0002 | c0004 | t0006 | g0311 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02257 | hp1 | a0013 | c0018 | t0001 | g0198 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02280 | hp1 | a0001 | c0003 | t0003 | g0112 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0241 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02451 | hp1 | a0005 | c0008 | t0001 | g0120 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02523 | hp2 | a0002 | c0004 | t0006 | g0317 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02602 | hp2 | a0001 | c0017 | t0003 | g0124 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02622 | hp1 | a0002 | c0004 | t0006 | g0300 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02622 | hp2 | a0012 | c0013 | t0012 | g0333 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02630 | hp1 | a0001 | c0003 | t0003 | g0154 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02647 | hp1 | a0001 | c0003 | t0008 | g0266 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0347 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0352 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02698 | hp2 | a0001 | c0003 | t0003 | g0169 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0249 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02735 | hp1 | a0006 | c0009 | t0001 | g0193 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0374 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02809 | hp2 | a0001 | c0007 | t0008 | g0342 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02818 | hp1 | a0010 | c0016 | t0006 | g0265 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0295 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0294 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0379 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0286 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02922 | hp2 | a0001 | c0007 | t0008 | g0280 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0329 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0282 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0319 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02976 | hp1 | a0001 | c0003 | t0008 | g0264 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03017 | hp1 | a0002 | c0004 | t0007 | g0217 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0278 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03098 | hp2 | a0011 | c0011 | t0004 | g0267 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03130 | hp2 | a0001 | c0003 | t0008 | g0263 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03139 | hp2 | a0001 | c0003 | t0008 | g0269 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03195 | hp1 | a0001 | c0003 | t0008 | g0262 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0380 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03225 | hp1 | a0008 | c0010 | t0004 | g0226 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03239 | hp1 | a0001 | c0003 | t0003 | g0183 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03239 | hp2 | a0001 | c0003 | t0003 | g0129 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0270 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03453 | hp2 | a0002 | c0004 | t0006 | g0224 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0382 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0279 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03490 | hp1 | a0001 | c0003 | t0003 | g0123 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03490 | hp2 | a0001 | c0003 | t0003 | g0005 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0014 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03492 | hp1 | a0001 | c0003 | t0003 | g0005 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03540 | hp1 | a0002 | c0004 | t0006 | g0225 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0378 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0370 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0349 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03688 | hp1 | a0001 | c0003 | t0003 | g0015 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0244 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0351 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0276 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03831 | hp2 | a0004 | c0006 | t0001 | g0383 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0356 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0245 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG04204 | hp1 | a0001 | c0003 | t0003 | g0168 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0230 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG04228 | hp2 | a0002 | c0004 | t0007 | g0111 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0268 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18612 | hp2 | a0002 | c0004 | t0007 | g0335 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18747 | hp2 | a0001 | c0003 | t0003 | g0128 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18939 | hp1 | a0001 | c0003 | t0003 | g0077 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18940 | hp2 | a0001 | c0003 | t0003 | g0180 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18941 | hp1 | a0002 | c0004 | t0006 | g0330 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18941 | hp2 | a0001 | c0003 | t0003 | g0176 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18942 | hp2 | a0002 | c0004 | t0006 | g0301 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18944 | hp1 | a0004 | c0006 | t0001 | g0213 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18944 | hp2 | a0003 | c0005 | t0002 | g0080 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18946 | hp2 | a0001 | c0003 | t0003 | g0163 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18947 | hp2 | a0002 | c0004 | t0007 | g0143 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18950 | hp2 | a0002 | c0004 | t0006 | g0303 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18952 | hp2 | a0002 | c0004 | t0006 | g0304 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18953 | hp1 | a0001 | c0003 | t0003 | g0170 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18953 | hp2 | a0002 | c0004 | t0007 | g0139 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18956 | hp1 | a0002 | c0004 | t0007 | g0130 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18956 | hp2 | a0001 | c0001 | t0013 | g0211 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18959 | hp1 | a0002 | c0004 | t0007 | g0140 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18960 | hp1 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18960 | hp2 | a0002 | c0004 | t0007 | g0141 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18961 | hp1 | a0001 | c0001 | t0009 | g0308 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18961 | hp2 | a0001 | c0003 | t0003 | g0173 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18962 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18964 | hp2 | a0002 | c0004 | t0007 | g0132 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0346 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18969 | hp2 | a0001 | c0003 | t0003 | g0145 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18971 | hp2 | a0003 | c0005 | t0002 | g0055 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18974 | hp1 | a0002 | c0004 | t0006 | g0313 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18979 | hp1 | a0001 | c0003 | t0003 | g0159 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0012 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18980 | hp2 | a0002 | c0004 | t0007 | g0131 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18983 | hp2 | a0003 | c0005 | t0002 | g0058 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18984 | hp1 | a0002 | c0004 | t0006 | g0315 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0012 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18985 | hp2 | a0002 | c0004 | t0007 | g0144 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18986 | hp2 | a0003 | c0005 | t0002 | g0171 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18988 | hp1 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18994 | hp2 | a0002 | c0004 | t0006 | g0314 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18995 | hp1 | a0001 | c0003 | t0003 | g0177 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18995 | hp2 | a0001 | c0003 | t0003 | g0178 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18997 | hp1 | a0001 | c0001 | t0009 | g0367 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18997 | hp2 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18998 | hp2 | a0002 | c0004 | t0006 | g0309 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18999 | hp1 | a0003 | c0005 | t0002 | g0072 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18999 | hp2 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19004 | hp2 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19005 | hp2 | a0001 | c0003 | t0008 | g0306 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19007 | hp1 | a0001 | c0003 | t0003 | g0033 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19009 | hp1 | a0003 | c0005 | t0002 | g0109 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0188 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19012 | hp1 | a0001 | c0003 | t0003 | g0153 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19030 | hp1 | a0001 | c0007 | t0008 | g0345 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19056 | hp1 | a0001 | c0003 | t0003 | g0223 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19056 | hp2 | a0002 | c0004 | t0006 | g0332 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19060 | hp1 | a0001 | c0003 | t0003 | g0162 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19063 | hp1 | a0002 | c0004 | t0006 | g0312 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19064 | hp1 | a0002 | c0004 | t0007 | g0133 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19065 | hp2 | a0004 | c0006 | t0001 | g0214 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19066 | hp1 | a0001 | c0014 | t0002 | g0036 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19066 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19067 | hp1 | a0002 | c0004 | t0006 | g0298 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19070 | hp1 | a0002 | c0004 | t0007 | g0032 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19074 | hp2 | a0001 | c0003 | t0003 | g0161 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19075 | hp2 | a0001 | c0003 | t0003 | g0187 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19077 | hp2 | a0002 | c0004 | t0006 | g0316 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19082 | hp1 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19082 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19085 | hp2 | a0002 | c0004 | t0006 | g0331 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19087 | hp1 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19090 | hp1 | a0001 | c0003 | t0003 | g0152 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19091 | hp2 | a0002 | c0004 | t0007 | g0017 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19240 | hp1 | a0001 | c0002 | t0004 | g0377 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ASW | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA20129 | hp2 | a0005 | c0008 | t0001 | g0118 | AFR | ASW | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0110 | EUR | TSI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA20805 | hp2 | a0004 | c0006 | t0001 | g0357 | EUR | TSI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0372 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02109 | hp1 | a0001 | c0003 | t0008 | g0334 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02486 | hp1 | a0001 | c0007 | t0008 | g0344 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03471 | hp1 | a0001 | c0007 | t0008 | g0343 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18955 | hp1 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA18955 | hp2 | a0002 | c0004 | t0006 | g0299 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA20300 | hp1 | a0001 | c0002 | t0004 | g0371 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
NA21309 | hp2 | a0007 | c0019 | t0008 | g0375 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
homoSapiens_chm13v2 | hp1 | a0009 | c0012 | t0001 | g0360 | REF | REF | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:72937972 | A | C | 2 | a0001a0003 | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
splice_region_variant | LOW | c.-7A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | chr14 | 72937972 | ||||||
chr14:72938010 | G | T | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.32G>T | p.Arg11Leu | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | 120/2474 | 32/1488 | 11/495 | chr14 | 72938010 | ||
chr14:72938044 | G | C | 2 | a0002a0008 | 45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
missense_variant | MODERATE | c.66G>C | p.Trp22Cys | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | 154/2474 | 66/1488 | 22/495 | chr14 | 72938044 | ||
chr14:72939813 | G | A | 1 | a0003 | 6 | NA18944.hp2 NA18971.hp2 NA18983.hp2 others(3): Show |
missense_variant | MODERATE | c.104G>A | p.Arg35Gln | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/14 | 192/2474 | 104/1488 | 35/495 | chr14 | 72939813 | ||
chr14:72943011 | G | A | 1 | a0009 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.449G>A | p.Arg150His | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/14 | 537/2474 | 449/1488 | 150/495 | chr14 | 72943011 | ||
chr14:72945927 | A | C | 2 | a0004a0006 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
missense_variant | MODERATE | c.578A>C | p.Lys193Thr | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/14 | 666/2474 | 578/1488 | 193/495 | chr14 | 72945927 | ||
chr14:72951866 | A | G | 1 | a0013 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.797A>G | p.Asn266Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/14 | 885/2474 | 797/1488 | 266/495 | chr14 | 72951866 | ||
chr14:72954442 | G | A | 1 | a0012 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.964G>A | p.Gly322Arg | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/14 | 1052/2474 | 964/1488 | 322/495 | chr14 | 72954442 | ||
chr14:72954478 | C | T | 1 | a0004 | 6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
missense_variant | MODERATE | c.1000C>T | p.Leu334Phe | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/14 | 1088/2474 | 1000/1488 | 334/495 | chr14 | 72954478 | ||
chr14:72955551 | C | G | 2 | a0002a0010 | 45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
missense_variant | MODERATE | c.1034C>G | p.Ser345Cys | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/14 | 1122/2474 | 1034/1488 | 345/495 | chr14 | 72955551 | ||
chr14:72958656 | C | T | 1 | a0011 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1339C>T | p.Arg447Cys | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1427/2474 | 1339/1488 | 447/495 | chr14 | 72958656 | ||
chr14:72958770 | G | A | 1 | a0005 | 2 | HG02451.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1453G>A | p.Val485Ile | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1541/2474 | 1453/1488 | 485/495 | chr14 | 72958770 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:72938062 | T | C | 1 | a0001c0007 | 5 | HG02486.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
synonymous_variant | LOW | c.84T>C | p.Ser28Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | 172/2474 | 84/1488 | 28/495 | chr14 | 72938062 | ||
chr14:72939874 | T | G | 1 | a0011c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.165T>G | p.Ser55Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/14 | 253/2474 | 165/1488 | 55/495 | chr14 | 72939874 | ||
chr14:72954243 | A | G | 1 | a0001c0017 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.888A>G | p.Ala296Ala | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/14 | 976/2474 | 888/1488 | 296/495 | chr14 | 72954243 | ||
chr14:72955642 | T | G | 2 | a0001c0002a0009c0012 | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
synonymous_variant | LOW | c.1125T>G | p.Ser375Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/14 | 1213/2474 | 1125/1488 | 375/495 | chr14 | 72955642 | ||
chr14:72956490 | C | A | 1 | a0001c0014 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.1284C>A | p.Ile428Ile | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/14 | 1372/2474 | 1284/1488 | 428/495 | chr14 | 72956490 | ||
chr14:72958724 | G | A | 1 | a0001c0015 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1407G>A | p.Ser469Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1495/2474 | 1407/1488 | 469/495 | chr14 | 72958724 | ||
chr14:72958754 | G | A | 3 | a0001c0003a0001c0015a0001c0017 | 61 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(58): Show |
synonymous_variant | LOW | c.1437G>A | p.Pro479Pro | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1525/2474 | 1437/1488 | 479/495 | chr14 | 72958754 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:72926538 | G | C | 11 | a0001c0001t0004a0001c0001t0009a0001c0002t0004others(8): Show | 91 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/14 | 11441 | chr14 | 72926538 | |||||
chr14:72958886 | G | T | 1 | a0001c0001t0011 | 2 | HG02723.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*81G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 81 | chr14 | 72958886 | |||||
chr14:72958973 | A | C | 8 | a0001c0001t0003a0001c0001t0005a0001c0003t0003others(5): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 168 | chr14 | 72958973 | |||||
chr14:72959130 | C | T | 1 | a0001c0001t0013 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 325 | chr14 | 72959130 | |||||
chr14:72959331 | C | G | 2 | a0001c0001t0010a0012c0013t0012 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*526C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 526 | chr14 | 72959331 | |||||
chr14:72959359 | C | G | 1 | a0001c0001t0005 | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*554C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 554 | chr14 | 72959359 | |||||
chr14:72959582 | C | T | 3 | a0002c0004t0006a0002c0004t0007a0010c0016t0006 | 45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*777C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 777 | chr14 | 72959582 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:72926576 | A | G | 167 | a0001c0001t0001g0251a0001c0001t0001g0284a0001c0001t0001g0336others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-9+33A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926576 | ||||||
chr14:72926593 | C | T | 1 | a0001c0003t0003g0223 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-9+50C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926593 | ||||||
chr14:72926650 | AAGGGGCG others(3): Show |
A | 3 | a0001c0003t0003g0013a0001c0003t0003g0014a0001c0003t0003g0015 | 3 | HG00642.hp1 HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-9+121_-9+130delGG others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72926650 | |||||
chr14:72926682 | C | T | 1 | a0004c0006t0001g0383 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-9+139C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926682 | ||||||
chr14:72926683 | G | A | 98 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(95): Show | 101 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-9+140G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926683 | ||||||
chr14:72926715 | A | C | 2 | a0001c0002t0004g0381a0001c0002t0004g0382 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+172A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926715 | ||||||
chr14:72926849 | A | C | 366 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(363): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-9+306A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926849 | ||||||
chr14:72926851 | C | T | 1 | a0001c0002t0001g0110 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-9+308C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926851 | ||||||
chr14:72926882 | G | A | 2 | a0001c0002t0001g0126a0001c0002t0001g0127 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9+339G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926882 | ||||||
chr14:72926962 | T | A | 1 | a0001c0003t0003g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-9+419T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926962 | ||||||
chr14:72927019 | A | G | 1 | a0002c0004t0007g0222 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-9+476A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927019 | ||||||
chr14:72927170 | G | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0134a0001c0001t0001g0135others(144): Show | 151 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-9+627G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927170 | ||||||
chr14:72927319 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-9+776G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927319 | ||||||
chr14:72927343 | C | CT | 12 | a0001c0001t0001g0004a0001c0001t0001g0125a0001c0002t0001g0221others(9): Show | 13 | HG00323.hp1 HG00733.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+828dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | |||||
chr14:72927343 | CTTTTTTT | C | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0002g0108others(4): Show | 7 | HG00408.hp1 HG00741.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+822_-9+828delTT others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | |||||
chr14:72927343 | CTTTTTTT others(1): Show |
C | 143 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+821_-9+828delTT others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | |||||
chr14:72927343 | CTTTTTTT others(2): Show |
C | 179 | a0001c0001t0001g0016a0001c0001t0001g0134a0001c0001t0001g0135others(176): Show | 189 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.-9+820_-9+828delTT others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | |||||
chr14:72927343 | CTTTTTTT others(3): Show |
C | 18 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(15): Show | 18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+819_-9+828delTT others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | |||||
chr14:72927371 | T | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0002c0004t0007g0111others(1): Show | 4 | HG01358.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+828T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927371 | ||||||
chr14:72927371 | T | TG | 3 | a0001c0001t0001g0219a0002c0004t0007g0218a0002c0004t0007g0220 | 3 | HG00735.hp2 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-9+829dupG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927371 | |||||
chr14:72927413 | A | G | 1 | a0002c0004t0007g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+870A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927413 | ||||||
chr14:72927414 | C | T | 294 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0192others(291): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-9+871C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927414 | ||||||
chr14:72927453 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-9+910G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927453 | ||||||
chr14:72927483 | C | T | 1 | a0001c0001t0011g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-9+940C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927483 | ||||||
chr14:72927572 | C | T | 3 | a0004c0006t0001g0011a0004c0006t0001g0214a0004c0006t0001g0383 | 4 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1029C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927572 | ||||||
chr14:72927602 | C | T | 1 | a0001c0003t0003g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9+1059C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927602 | ||||||
chr14:72927629 | G | C | 4 | a0002c0004t0007g0130a0002c0004t0007g0131a0002c0004t0007g0132others(1): Show | 4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1086G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927629 | ||||||
chr14:72927630 | C | A | 4 | a0002c0004t0007g0130a0002c0004t0007g0131a0002c0004t0007g0132others(1): Show | 4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1087C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927630 | ||||||
chr14:72927631 | G | C | 4 | a0002c0004t0007g0130a0002c0004t0007g0131a0002c0004t0007g0132others(1): Show | 4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1088G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927631 | ||||||
chr14:72927633 | G | T | 4 | a0002c0004t0007g0130a0002c0004t0007g0131a0002c0004t0007g0132others(1): Show | 4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1090G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927633 | ||||||
chr14:72927634 | AGCCACCG others(20): Show |
A | 4 | a0002c0004t0007g0130a0002c0004t0007g0131a0002c0004t0007g0132others(1): Show | 4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1092_-9+1118del others(27): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927634 | ||||||
chr14:72927640 | C | T | 2 | a0001c0001t0002g0107a0001c0001t0009g0281 | 2 | HG01175.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+1097C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927640 | ||||||
chr14:72927641 | G | A | 1 | a0001c0001t0002g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-9+1098G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927641 | ||||||
chr14:72927662 | T | C | 4 | a0002c0004t0007g0130a0002c0004t0007g0131a0002c0004t0007g0132others(1): Show | 4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1119T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927662 | ||||||
chr14:72927906 | G | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0251a0001c0001t0001g0336others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-9+1363G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927906 | ||||||
chr14:72927972 | G | A | 170 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0192others(167): Show | 177 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.-9+1429G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927972 | ||||||
chr14:72927994 | T | C | 61 | a0001c0001t0002g0175a0001c0001t0002g0182a0001c0002t0001g0181others(58): Show | 62 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+1451T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927994 | ||||||
chr14:72928054 | G | C | 1 | a0001c0001t0009g0346 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-9+1511G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928054 | ||||||
chr14:72928060 | C | G | 67 | a0001c0001t0002g0175a0001c0001t0002g0182a0001c0002t0001g0181others(64): Show | 68 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-9+1517C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928060 | ||||||
chr14:72928117 | A | C | 1 | a0001c0003t0003g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-9+1574A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928117 | ||||||
chr14:72928187 | C | CT | 13 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0122others(10): Show | 15 | HG00323.hp1 HG01168.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+1667dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTT | 61 | a0001c0001t0001g0216a0001c0001t0001g0284a0001c0001t0004g0283others(58): Show | 62 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-9+1663_-9+1667dup others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTT | 11 | a0001c0001t0001g0016a0001c0001t0001g0197a0001c0001t0002g0175others(8): Show | 11 | HG00423.hp2 HG02055.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+1662_-9+1667dup others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(3): Show |
3 | a0001c0003t0008g0262a0001c0003t0008g0263a0001c0003t0008g0264 | 3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-9+1658_-9+1667dup others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0047a0001c0001t0004g0318a0001c0002t0001g0200others(5): Show | 8 | HG01081.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1657_-9+1667dup others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(5): Show |
35 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0004g0252others(32): Show | 36 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-9+1656_-9+1667dup others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(6): Show |
30 | a0001c0001t0001g0048a0001c0001t0002g0025a0001c0001t0002g0035others(27): Show | 31 | HG00323.hp2 HG00558.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-9+1655_-9+1667dup others(13): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(7): Show |
43 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(40): Show | 47 | HG00738.hp2 HG00741.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9+1654_-9+1667dup others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(8): Show |
40 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0192others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+1653_-9+1667dup others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(9): Show |
16 | a0001c0001t0002g0002a0001c0001t0002g0046a0001c0001t0002g0092others(13): Show | 17 | HG00642.hp2 HG00735.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9+1652_-9+1667dup others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0251a0001c0001t0002g0098a0001c0001t0002g0099others(3): Show | 6 | HG02004.hp2 HG02074.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1651_-9+1667dup others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104 | 3 | NA18970.hp1 NA18970.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-9+1650_-9+1667dup others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0002t0004g0319others(1): Show | 4 | HG02132.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1649_-9+1667dup others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(13): Show |
4 | a0001c0002t0004g0376a0001c0002t0004g0377a0001c0002t0004g0378others(1): Show | 4 | HG01496.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1648_-9+1667dup others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(14): Show |
3 | a0001c0002t0004g0268a0001c0002t0004g0371a0001c0002t0004g0380 | 3 | HG03209.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-9+1647_-9+1667dup others(21): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | C | CTTTTTTT others(19): Show |
1 | a0001c0002t0004g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9+1667_-9+1668ins others(26): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928187 | CT | C | 39 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(36): Show | 40 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+1667delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | |||||
chr14:72928279 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-9+1736C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928279 | ||||||
chr14:72928280 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9+1737G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928280 | ||||||
chr14:72928312 | G | C | 1 | a0001c0001t0001g0366 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-9+1769G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928312 | ||||||
chr14:72928334 | C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0219 | 3 | HG02258.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+1791C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928334 | ||||||
chr14:72928361 | C | T | 367 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(364): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-9+1818C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928361 | ||||||
chr14:72928382 | C | T | 1 | a0001c0001t0005g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-9+1839C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928382 | ||||||
chr14:72928406 | A | C | 1 | a0001c0003t0003g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-9+1863A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928406 | ||||||
chr14:72928408 | G | C | 1 | a0001c0001t0005g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-9+1865G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928408 | ||||||
chr14:72928416 | A | G | 9 | a0001c0001t0001g0197a0001c0001t0004g0286a0001c0001t0004g0287others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+1873A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928416 | ||||||
chr14:72928438 | G | T | 4 | a0001c0007t0008g0342a0001c0007t0008g0343a0001c0007t0008g0344others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+1895G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928438 | ||||||
chr14:72928452 | C | T | 1 | a0001c0002t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+1909C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928452 | ||||||
chr14:72928465 | G | T | 1 | a0001c0002t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-9+1922G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928465 | ||||||
chr14:72928511 | C | A | 1 | a0001c0001t0001g0004 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-9+1968C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928511 | ||||||
chr14:72928556 | C | T | 2 | a0002c0004t0007g0139a0002c0004t0007g0141 | 2 | NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-9+2013C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928556 | ||||||
chr14:72928562 | C | T | 39 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0339others(36): Show | 40 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.-9+2019C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928562 | ||||||
chr14:72928585 | T | TTATATAT others(41): Show |
1 | a0001c0007t0008g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+2074_-9+2075ins others(48): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | T | TTTTATAT others(1): Show |
5 | a0001c0001t0003g0250a0001c0007t0008g0342a0001c0007t0008g0343others(2): Show | 5 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | T | TTTTATAT others(3): Show |
27 | a0001c0001t0001g0337a0001c0001t0005g0006a0001c0001t0005g0034others(24): Show | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | T | TTTTATAT others(5): Show |
6 | a0001c0001t0001g0336a0001c0001t0001g0339a0001c0001t0001g0340others(3): Show | 6 | HG02723.hp1 HG03942.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | T | TTTTATAT others(13): Show |
1 | a0001c0003t0008g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | TTA | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0122others(2): Show | 6 | HG00733.hp2 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2073_-9+2074del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | TTATA | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0215others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2071_-9+2074del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | TTATATA | T | 8 | a0001c0001t0001g0016a0001c0001t0010g0278a0001c0001t0010g0279others(5): Show | 8 | HG02109.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+2069_-9+2074del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | TTATATAT others(1): Show |
T | 12 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0138others(9): Show | 12 | HG01081.hp1 HG01106.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+2067_-9+2074del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | TTATATAT others(3): Show |
T | 74 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(71): Show | 75 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+2065_-9+2074del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928585 | TTATATAT others(5): Show |
T | 229 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0192others(226): Show | 238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-9+2063_-9+2074del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | |||||
chr14:72928587 | A | T | 2 | a0001c0001t0005g0246a0001c0003t0003g0173 | 2 | NA18961.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-9+2044A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928587 | ||||||
chr14:72928591 | A | T | 3 | a0001c0001t0001g0191a0001c0001t0004g0318a0001c0003t0008g0266 | 3 | HG02647.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+2048A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928591 | ||||||
chr14:72928593 | A | T | 6 | a0001c0001t0001g0016a0001c0003t0008g0262a0001c0003t0008g0263others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2050A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928593 | ||||||
chr14:72928594 | T | A | 5 | a0001c0001t0001g0336a0001c0001t0001g0339a0001c0001t0001g0340others(2): Show | 5 | HG03942.hp1 NA18947.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2051T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928594 | ||||||
chr14:72928594 | T | TATATATA others(4): Show |
1 | a0001c0001t0005g0246 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9+2052_-9+2062dup others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928594 | |||||
chr14:72928595 | A | T | 12 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0138others(9): Show | 12 | HG01081.hp1 HG01106.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+2052A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928595 | ||||||
chr14:72928596 | T | A | 28 | a0001c0001t0001g0337a0001c0001t0005g0006a0001c0001t0005g0034others(25): Show | 29 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+2053T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928596 | ||||||
chr14:72928597 | A | T | 72 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(69): Show | 73 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-9+2054A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928597 | ||||||
chr14:72928598 | T | A | 5 | a0001c0001t0003g0250a0001c0007t0008g0342a0001c0007t0008g0343others(2): Show | 5 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2055T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928598 | ||||||
chr14:72928599 | A | T | 229 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0192others(226): Show | 238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-9+2056A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928599 | ||||||
chr14:72928611 | A | G | 2 | a0006c0009t0001g0193a0006c0009t0001g0194 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-9+2068A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928611 | ||||||
chr14:72928627 | C | A | 4 | a0001c0007t0008g0342a0001c0007t0008g0343a0001c0007t0008g0344others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2084C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928627 | ||||||
chr14:72928777 | A | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+2234A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928777 | ||||||
chr14:72928874 | C | G | 1 | a0001c0001t0004g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+2331C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928874 | ||||||
chr14:72928971 | C | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0076others(2): Show | 5 | NA18939.hp1 NA18961.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+2428C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928971 | ||||||
chr14:72928976 | C | T | 2 | a0006c0009t0001g0193a0006c0009t0001g0194 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-9+2433C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928976 | ||||||
chr14:72928977 | A | AG | 211 | a0001c0001t0001g0016a0001c0001t0001g0134a0001c0001t0001g0135others(208): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-9+2438dupG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928977 | |||||
chr14:72929079 | C | A | 316 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0134others(313): Show | 326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.-9+2536C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929079 | ||||||
chr14:72929108 | C | G | 2 | a0001c0003t0008g0269a0001c0007t0008g0280 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-9+2565C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929108 | ||||||
chr14:72929127 | C | T | 2 | a0001c0003t0008g0269a0001c0007t0008g0280 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-9+2584C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929127 | ||||||
chr14:72929216 | G | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0219 | 3 | HG02258.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+2673G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929216 | ||||||
chr14:72929295 | A | G | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+2752A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929295 | ||||||
chr14:72929298 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+2755C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929298 | ||||||
chr14:72929312 | C | T | 1 | a0002c0004t0006g0307 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+2769C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929312 | ||||||
chr14:72929423 | C | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+2880C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929423 | ||||||
chr14:72929532 | T | C | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+2989T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929532 | ||||||
chr14:72929533 | C | G | 102 | a0001c0001t0001g0078a0001c0001t0001g0251a0001c0001t0002g0001others(99): Show | 106 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-9+2990C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929533 | ||||||
chr14:72929739 | A | G | 375 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0047others(372): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-9+3196A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929739 | ||||||
chr14:72929779 | C | T | 1 | a0002c0004t0007g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-9+3236C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929779 | ||||||
chr14:72929836 | CGCCCGCG others(11): Show |
C | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+3297_-9+3314del others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72929836 | |||||
chr14:72929956 | G | A | 6 | a0002c0004t0007g0111a0002c0004t0007g0114a0002c0004t0007g0217others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3413G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929956 | ||||||
chr14:72930112 | G | A | 1 | a0001c0014t0002g0036 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-9+3569G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930112 | ||||||
chr14:72930113 | G | T | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-9+3570G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930113 | ||||||
chr14:72930154 | G | A | 1 | a0001c0001t0009g0295 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+3611G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930154 | ||||||
chr14:72930155 | T | C | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3612T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930155 | ||||||
chr14:72930246 | C | CT | 87 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0191others(84): Show | 89 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-9+3715dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72930246 | |||||
chr14:72930246 | C | CTT | 79 | a0001c0001t0001g0137a0001c0001t0001g0197a0001c0001t0001g0216others(76): Show | 82 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-9+3714_-9+3715dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72930246 | |||||
chr14:72930254 | T | C | 101 | a0001c0001t0001g0078a0001c0001t0001g0251a0001c0001t0002g0001others(98): Show | 105 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-9+3711T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930254 | ||||||
chr14:72930259 | G | C | 1 | a0001c0001t0002g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9+3716G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930259 | ||||||
chr14:72930309 | C | A | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+3766C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930309 | ||||||
chr14:72930511 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-9+3968C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930511 | ||||||
chr14:72930641 | G | GTA | 131 | a0001c0001t0001g0016a0001c0001t0001g0137a0001c0001t0001g0197others(128): Show | 136 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+4110_-9+4111dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72930641 | |||||
chr14:72930713 | G | A | 3 | a0001c0001t0003g0250a0001c0001t0011g0249a0001c0001t0011g0270 | 3 | HG01074.hp2 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+4170G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930713 | ||||||
chr14:72931263 | C | CT | 244 | a0001c0001t0001g0016a0001c0001t0001g0136a0001c0001t0001g0197others(241): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-9+4738dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | |||||
chr14:72931263 | C | CTT | 9 | a0001c0001t0002g0031a0001c0001t0002g0071a0001c0001t0002g0101others(6): Show | 9 | HG02074.hp2 HG02970.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+4737_-9+4738dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | |||||
chr14:72931263 | C | CTTT | 42 | a0001c0003t0008g0306a0002c0004t0006g0009a0002c0004t0006g0224others(39): Show | 43 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-9+4736_-9+4738dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | |||||
chr14:72931263 | C | CTTTT | 8 | a0002c0004t0006g0316a0002c0004t0006g0331a0002c0004t0006g0332others(5): Show | 8 | HG00323.hp1 HG02735.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+4735_-9+4738dup others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | |||||
chr14:72931263 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-9+4720C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931263 | ||||||
chr14:72931265 | T | C | 1 | a0001c0007t0008g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+4722T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931265 | ||||||
chr14:72931737 | A | C | 1 | a0001c0003t0003g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-9+5194A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931737 | ||||||
chr14:72931738 | G | A | 45 | a0001c0003t0008g0306a0002c0004t0006g0009a0002c0004t0006g0224others(42): Show | 46 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-9+5195G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931738 | ||||||
chr14:72931873 | G | A | 2 | a0004c0006t0001g0213a0004c0006t0001g0214 | 2 | NA18944.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-9+5330G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931873 | ||||||
chr14:72931883 | G | A | 1 | a0001c0002t0004g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9+5340G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931883 | ||||||
chr14:72931951 | CTG | C | 5 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(2): Show | 6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+5410_-9+5411del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931951 | |||||
chr14:72931985 | CTTCT | C | 15 | a0001c0001t0003g0250a0001c0001t0011g0249a0001c0001t0011g0270others(12): Show | 15 | HG01074.hp2 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+5445_-9+5448del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931985 | |||||
chr14:72931987 | TC | T | 32 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0336others(29): Show | 33 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.-9+5445delC | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931987 | ||||||
chr14:72931988 | C | T | 2 | a0001c0001t0001g0341a0001c0001t0005g0276 | 2 | HG03831.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-9+5445C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931988 | ||||||
chr14:72931988 | CT | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0047others(134): Show | 144 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+5461delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931988 | |||||
chr14:72932007 | G | A | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+5464G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932007 | ||||||
chr14:72932191 | A | G | 1 | a0001c0003t0003g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-9+5648A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932191 | ||||||
chr14:72932477 | C | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | NA18950.hp1 NA18963.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-8-5494C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932477 | ||||||
chr14:72932710 | T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-5261T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932710 | ||||||
chr14:72932810 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-8-5161C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932810 | ||||||
chr14:72932880 | TTTTC | T | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-5071_-8-5068del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72932880 | |||||
chr14:72932946 | G | A | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-5025G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932946 | ||||||
chr14:72932998 | C | T | 130 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(127): Show | 134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-8-4973C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932998 | ||||||
chr14:72933129 | A | G | 45 | a0001c0003t0008g0306a0002c0004t0006g0009a0002c0004t0006g0224others(42): Show | 46 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-8-4842A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933129 | ||||||
chr14:72933140 | A | AC | 53 | a0001c0003t0003g0005a0001c0003t0003g0013a0001c0003t0003g0014others(50): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-4827dupC | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72933140 | |||||
chr14:72933142 | C | T | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-4829C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933142 | ||||||
chr14:72933330 | A | G | 353 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(350): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-8-4641A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933330 | ||||||
chr14:72933558 | CA | C | 132 | a0001c0001t0001g0016a0001c0001t0001g0197a0001c0001t0001g0216others(129): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-8-4397delA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72933558 | |||||
chr14:72933664 | C | T | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-4307C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933664 | ||||||
chr14:72933816 | C | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-4155C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933816 | ||||||
chr14:72933922 | G | A | 1 | a0001c0002t0001g0097 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-8-4049G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933922 | ||||||
chr14:72933973 | C | T | 11 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(8): Show | 11 | HG00544.hp2 HG01081.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-3998C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933973 | ||||||
chr14:72934132 | C | T | 252 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(249): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-8-3839C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934132 | ||||||
chr14:72934156 | C | CT | 18 | a0001c0001t0003g0250a0001c0001t0004g0287a0001c0001t0011g0249others(15): Show | 18 | HG01074.hp2 HG02109.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-3801dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72934156 | |||||
chr14:72934156 | C | CTT | 60 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-8-3802_-8-3801dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72934156 | |||||
chr14:72934156 | C | CTTT | 54 | a0001c0001t0001g0341a0001c0001t0005g0244a0001c0003t0003g0005others(51): Show | 55 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-8-3803_-8-3801dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72934156 | |||||
chr14:72934239 | C | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-3732C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934239 | ||||||
chr14:72934266 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-3705G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934266 | ||||||
chr14:72934298 | C | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-3673C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934298 | ||||||
chr14:72934388 | A | G | 1 | a0007c0019t0008g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-3583A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934388 | ||||||
chr14:72934447 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-3524C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934447 | ||||||
chr14:72934449 | C | T | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-3522C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934449 | ||||||
chr14:72934487 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-8-3484G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934487 | ||||||
chr14:72934488 | T | C | 353 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(350): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-8-3483T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934488 | ||||||
chr14:72934496 | G | T | 2 | a0001c0002t0001g0200a0001c0002t0004g0294 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-3475G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934496 | ||||||
chr14:72934584 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8-3387C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934584 | ||||||
chr14:72934886 | C | T | 1 | a0002c0004t0007g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-8-3085C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934886 | ||||||
chr14:72934912 | C | A | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-3059C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934912 | ||||||
chr14:72934943 | A | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-3028A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934943 | ||||||
chr14:72935059 | A | G | 1 | a0001c0003t0008g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-8-2912A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935059 | ||||||
chr14:72935158 | T | A | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-2813T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935158 | ||||||
chr14:72935197 | T | C | 253 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-8-2774T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935197 | ||||||
chr14:72935261 | A | ATTT | 341 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(338): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-8-2701_-8-2699dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72935261 | |||||
chr14:72935261 | A | ATTTT | 19 | a0001c0001t0005g0243a0001c0001t0009g0346a0001c0002t0001g0207others(16): Show | 19 | HG00423.hp1 HG00741.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-2702_-8-2699dup others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72935261 | |||||
chr14:72935278 | G | A | 5 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0221others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2693G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935278 | ||||||
chr14:72935344 | A | T | 253 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-8-2627A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935344 | ||||||
chr14:72935443 | C | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-2528C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935443 | ||||||
chr14:72935502 | G | A | 2 | a0001c0003t0003g0149a0013c0018t0001g0198 | 2 | HG02083.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-8-2469G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935502 | ||||||
chr14:72935619 | G | A | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-2352G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935619 | ||||||
chr14:72935643 | G | A | 252 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(249): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-8-2328G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935643 | ||||||
chr14:72935766 | T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-2205T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935766 | ||||||
chr14:72935958 | CTT | C | 7 | a0001c0003t0008g0262a0001c0003t0008g0263a0001c0003t0008g0264others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-2009_-8-2008del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72935958 | |||||
chr14:72936119 | G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-1852G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936119 | ||||||
chr14:72936225 | C | G | 183 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(180): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8-1746C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936225 | ||||||
chr14:72936306 | G | T | 1 | a0007c0019t0008g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-1665G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936306 | ||||||
chr14:72936409 | C | G | 1 | a0001c0003t0003g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8-1562C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936409 | ||||||
chr14:72936420 | T | C | 1 | a0007c0019t0008g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-1551T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936420 | ||||||
chr14:72936444 | G | T | 1 | a0001c0003t0003g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8-1527G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936444 | ||||||
chr14:72936563 | C | CA | 267 | a0001c0001t0001g0016a0001c0001t0001g0134a0001c0001t0001g0189others(264): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.-8-1392dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72936563 | |||||
chr14:72936613 | T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-1358T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936613 | ||||||
chr14:72936699 | G | A | 1 | a0003c0005t0002g0058 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-8-1272G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936699 | ||||||
chr14:72936823 | A | C | 4 | a0001c0007t0008g0342a0001c0007t0008g0343a0001c0007t0008g0344others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1148A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936823 | ||||||
chr14:72936840 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-8-1131A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936840 | ||||||
chr14:72936849 | G | T | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-1122G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936849 | ||||||
chr14:72936858 | A | G | 12 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0056others(9): Show | 13 | NA18943.hp2 NA18963.hp1 NA18971.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-1113A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936858 | ||||||
chr14:72936879 | T | C | 366 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(363): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-8-1092T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936879 | ||||||
chr14:72937001 | T | TG | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-970_-8-969insG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937001 | ||||||
chr14:72937129 | A | G | 1 | a0012c0013t0012g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-842A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937129 | ||||||
chr14:72937199 | GAGA | G | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-769_-8-767delAA others(1): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937199 | |||||
chr14:72937220 | G | C | 2 | a0002c0004t0006g0297a0002c0004t0006g0307 | 2 | HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-8-751G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937220 | ||||||
chr14:72937227 | CAGAT | C | 368 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(365): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.-8-739_-8-736delAG others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937227 | |||||
chr14:72937410 | C | CT | 153 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0336others(150): Show | 158 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-8-541dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937410 | |||||
chr14:72937410 | C | CTT | 62 | a0001c0001t0001g0341a0001c0001t0002g0031a0001c0001t0002g0050others(59): Show | 63 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-8-542_-8-541dupTT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937410 | |||||
chr14:72937410 | CT | C | 49 | a0001c0003t0003g0145a0001c0003t0003g0151a0002c0004t0006g0009others(46): Show | 51 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-541delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937410 | |||||
chr14:72937570 | G | A | 1 | a0002c0004t0007g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8-401G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937570 | ||||||
chr14:72937582 | G | A | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-389G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937582 | ||||||
chr14:72937661 | C | T | 1 | a0001c0003t0003g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-310C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937661 | ||||||
chr14:72937685 | C | T | 1 | a0001c0002t0004g0380 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-286C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937685 | ||||||
chr14:72937730 | G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-241G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937730 | ||||||
chr14:72937822 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-149A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937822 | ||||||
chr14:72937826 | A | C | 1 | a0001c0002t0001g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8-145A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937826 | ||||||
chr14:72937891 | G | A | 5 | a0001c0003t0008g0262a0001c0003t0008g0263a0001c0003t0008g0264others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-80G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937891 | ||||||
chr14:72937930 | AC | A | 11 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(8): Show | 11 | HG00544.hp2 HG01081.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-40delC | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937930 | ||||||
chr14:72937968 | T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02572.hp2 HG06807.hp1 |
splice_region_variant&intron_variant | LOW | c.-8-3T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937968 | ||||||
chr14:72938077 | G | A | 1 | a0003c0005t0002g0058 | 1 | NA18983.hp2 | splice_region_variant&intron_variant | LOW | c.92+7G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938077 | ||||||
chr14:72938087 | G | A | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.92+17G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938087 | ||||||
chr14:72938117 | G | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.92+47G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938117 | ||||||
chr14:72938260 | G | A | 2 | a0002c0004t0006g0224a0002c0004t0006g0225 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.92+190G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938260 | ||||||
chr14:72938369 | G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0199others(2): Show | 6 | HG00733.hp2 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+299G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938369 | ||||||
chr14:72938393 | G | A | 2 | a0001c0003t0003g0150a0001c0003t0003g0152 | 2 | NA18954.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.92+323G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938393 | ||||||
chr14:72938524 | T | A | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+454T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938524 | ||||||
chr14:72938533 | G | A | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.92+463G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938533 | ||||||
chr14:72938607 | A | G | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.92+537A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938607 | ||||||
chr14:72938732 | T | C | 1 | a0001c0001t0004g0289 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92+662T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938732 | ||||||
chr14:72938754 | T | C | 8 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0336others(5): Show | 8 | HG00408.hp1 HG01975.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+684T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938754 | ||||||
chr14:72938759 | G | A | 1 | a0001c0003t0008g0334 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+689G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938759 | ||||||
chr14:72938765 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+695C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938765 | ||||||
chr14:72938863 | T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.92+793T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938863 | ||||||
chr14:72938928 | C | G | 1 | a0001c0001t0002g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.92+858C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938928 | ||||||
chr14:72939070 | T | C | 2 | a0001c0003t0003g0153a0001c0003t0003g0177 | 2 | NA18995.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.93-732T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939070 | ||||||
chr14:72939460 | C | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0044 | 2 | NA19081.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.93-342C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939460 | ||||||
chr14:72939524 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.93-278A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939524 | ||||||
chr14:72939540 | A | G | 1 | a0002c0004t0006g0305 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.93-262A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939540 | ||||||
chr14:72939960 | C | T | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(96): Show | 103 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.193+58C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72939960 | ||||||
chr14:72939999 | C | T | 1 | a0001c0007t0008g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193+97C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72939999 | ||||||
chr14:72940022 | G | T | 1 | a0001c0001t0005g0241 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.193+120G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72940022 | ||||||
chr14:72940054 | C | T | 1 | a0001c0001t0004g0008 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.193+152C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72940054 | ||||||
chr14:72940147 | G | A | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(7): Show | 10 | HG00544.hp2 HG01081.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-73G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72940147 | ||||||
chr14:72940413 | G | A | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+36G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940413 | ||||||
chr14:72940550 | G | A | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.351+173G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940550 | ||||||
chr14:72940582 | C | G | 1 | a0002c0004t0007g0222 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.351+205C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940582 | ||||||
chr14:72940588 | G | GT | 66 | a0001c0001t0002g0096a0001c0001t0009g0281a0001c0002t0001g0010others(63): Show | 67 | HG00099.hp2 HG00558.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.351+213dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940588 | |||||
chr14:72940588 | G | GTT | 4 | a0001c0002t0001g0024a0001c0002t0001g0205a0001c0002t0001g0328others(1): Show | 4 | HG00323.hp2 HG03492.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+212_351+213dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940588 | |||||
chr14:72940590 | TG | T | 10 | a0001c0001t0001g0078a0001c0001t0001g0135a0001c0001t0001g0137others(7): Show | 10 | HG00544.hp2 HG02056.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+214delG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940590 | ||||||
chr14:72940591 | G | GT | 29 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0219others(26): Show | 31 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.351+231dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940591 | |||||
chr14:72940591 | G | GTT | 37 | a0002c0004t0006g0009a0002c0004t0006g0297a0002c0004t0006g0298others(34): Show | 38 | HG00423.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.351+230_351+231dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940591 | |||||
chr14:72940591 | G | GTTT | 6 | a0002c0004t0006g0225a0002c0004t0006g0310a0002c0004t0006g0312others(3): Show | 6 | HG00735.hp2 HG01358.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+229_351+231dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940591 | |||||
chr14:72940591 | G | T | 175 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0134others(172): Show | 180 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.351+214G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940591 | ||||||
chr14:72940596 | T | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0101a0013c0018t0001g0198 | 3 | HG02074.hp2 HG02155.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.351+219T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940596 | ||||||
chr14:72940686 | A | G | 365 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(362): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.351+309A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940686 | ||||||
chr14:72940692 | G | A | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.351+315G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940692 | ||||||
chr14:72940791 | A | C | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.351+414A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940791 | ||||||
chr14:72940881 | A | G | 368 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0048others(365): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.351+504A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940881 | ||||||
chr14:72940906 | A | G | 4 | a0001c0003t0008g0262a0001c0003t0008g0263a0001c0003t0008g0264others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+529A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940906 | ||||||
chr14:72940974 | G | GT | 352 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(349): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.351+604dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940974 | |||||
chr14:72941138 | A | AT | 4 | a0001c0003t0003g0005a0001c0003t0003g0166a0001c0003t0003g0167others(1): Show | 5 | HG00140.hp1 HG01433.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-599dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72941138 | |||||
chr14:72941148 | T | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(99): Show | 106 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.352-597T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941148 | ||||||
chr14:72941186 | G | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(99): Show | 106 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.352-559G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941186 | ||||||
chr14:72941208 | C | A | 2 | a0001c0001t0004g0256a0001c0001t0004g0329 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.352-537C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941208 | ||||||
chr14:72941426 | G | A | 129 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.352-319G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941426 | ||||||
chr14:72941578 | C | T | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.352-167C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941578 | ||||||
chr14:72941589 | G | T | 1 | a0001c0001t0002g0096 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.352-156G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941589 | ||||||
chr14:72941611 | A | AT | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(97): Show | 104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.352-129dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72941611 | |||||
chr14:72941647 | G | A | 254 | a0001c0001t0001g0016a0001c0001t0001g0189a0001c0001t0001g0192others(251): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.352-98G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941647 | ||||||
chr14:72941661 | A | AT | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.352-83dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72941661 | |||||
chr14:72941908 | G | C | 39 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(36): Show | 40 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.431+84G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72941908 | ||||||
chr14:72942002 | C | T | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431+178C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942002 | ||||||
chr14:72942063 | C | T | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+239C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942063 | ||||||
chr14:72942181 | A | G | 1 | a0001c0002t0004g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.431+357A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942181 | ||||||
chr14:72942309 | C | A | 1 | a0005c0008t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.431+485C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942309 | ||||||
chr14:72942415 | A | C | 1 | a0001c0001t0002g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.432-579A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942415 | ||||||
chr14:72942456 | C | T | 2 | a0004c0006t0001g0213a0004c0006t0001g0214 | 2 | NA18944.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.432-538C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942456 | ||||||
chr14:72942477 | C | T | 2 | a0001c0001t0001g0197a0001c0001t0004g0286 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.432-517C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942477 | ||||||
chr14:72942603 | G | GGCCGTAT others(19): Show |
1 | a0004c0006t0001g0357 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432-368_432-343dup others(26): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 72942603 | |||||
chr14:72942603 | GGCCGTAT others(19): Show |
G | 70 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(67): Show | 71 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.432-368_432-343del others(26): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 72942603 | |||||
chr14:72942638 | C | T | 2 | a0001c0001t0011g0249a0001c0001t0011g0270 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.432-356C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942638 | ||||||
chr14:72942687 | C | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-307C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942687 | ||||||
chr14:72942814 | T | C | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-180T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942814 | ||||||
chr14:72942832 | C | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-162C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942832 | ||||||
chr14:72942905 | G | A | 70 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(67): Show | 71 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.432-89G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942905 | ||||||
chr14:72942933 | C | T | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.432-61C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942933 | ||||||
chr14:72942953 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.432-41G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942953 | ||||||
chr14:72942975 | C | G | 146 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(143): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.432-19C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942975 | ||||||
chr14:72943182 | G | A | 1 | a0001c0003t0003g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.534+86G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943182 | ||||||
chr14:72943249 | G | C | 27 | a0001c0001t0005g0006a0001c0001t0005g0034a0001c0001t0005g0231others(24): Show | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+153G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943249 | ||||||
chr14:72943268 | A | C | 5 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0221others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+172A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943268 | ||||||
chr14:72943328 | G | A | 1 | a0001c0001t0002g0364 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.534+232G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943328 | ||||||
chr14:72943490 | C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(100): Show | 107 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.534+394C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943490 | ||||||
chr14:72943514 | G | A | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+418G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943514 | ||||||
chr14:72943750 | C | T | 1 | a0001c0001t0004g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.534+654C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943750 | ||||||
chr14:72943795 | G | A | 1 | a0001c0001t0005g0275 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.534+699G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943795 | ||||||
chr14:72943859 | G | A | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+763G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943859 | ||||||
chr14:72943913 | C | T | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.534+817C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943913 | ||||||
chr14:72943934 | T | G | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.534+838T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943934 | ||||||
chr14:72943942 | G | A | 1 | a0001c0001t0005g0272 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.534+846G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943942 | ||||||
chr14:72943961 | C | T | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+865C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943961 | ||||||
chr14:72943989 | G | T | 2 | a0001c0001t0002g0104a0001c0001t0002g0106 | 2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.534+893G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943989 | ||||||
chr14:72944085 | C | T | 4 | a0001c0003t0003g0112a0001c0003t0003g0113a0001c0003t0003g0123others(1): Show | 4 | HG02129.hp2 HG02280.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+989C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944085 | ||||||
chr14:72944337 | C | A | 27 | a0001c0001t0005g0006a0001c0001t0005g0034a0001c0001t0005g0231others(24): Show | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+1241C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944337 | ||||||
chr14:72944389 | C | T | 5 | a0001c0007t0008g0280a0001c0007t0008g0342a0001c0007t0008g0343others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+1293C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944389 | ||||||
chr14:72944690 | G | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(100): Show | 107 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.535-1194G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944690 | ||||||
chr14:72944736 | G | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0219 | 3 | HG02258.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.535-1148G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944736 | ||||||
chr14:72944782 | A | T | 23 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(20): Show | 23 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.535-1102A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944782 | ||||||
chr14:72944816 | T | C | 246 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(243): Show | 253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.535-1068T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944816 | ||||||
chr14:72944851 | G | A | 1 | a0002c0004t0006g0298 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.535-1033G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944851 | ||||||
chr14:72945068 | G | A | 1 | a0001c0003t0003g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.535-816G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945068 | ||||||
chr14:72945305 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.535-579A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945305 | ||||||
chr14:72945395 | T | TA | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.535-480dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 72945395 | |||||
chr14:72945463 | T | G | 37 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(34): Show | 38 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.535-421T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945463 | ||||||
chr14:72945474 | T | TA | 44 | a0001c0001t0003g0250a0002c0004t0006g0009a0002c0004t0006g0224others(41): Show | 45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.535-395dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 72945474 | |||||
chr14:72945474 | TA | T | 75 | a0001c0001t0001g0199a0001c0001t0002g0088a0001c0002t0001g0010others(72): Show | 76 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.535-395delA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 72945474 | |||||
chr14:72945491 | A | T | 27 | a0001c0001t0005g0006a0001c0001t0005g0034a0001c0001t0005g0231others(24): Show | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.535-393A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945491 | ||||||
chr14:72945528 | C | T | 1 | a0001c0003t0003g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.535-356C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945528 | ||||||
chr14:72945531 | C | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(98): Show | 105 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.535-353C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945531 | ||||||
chr14:72945727 | G | A | 1 | a0002c0004t0007g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.535-157G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945727 | ||||||
chr14:72945753 | C | A | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.535-131C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945753 | ||||||
chr14:72945756 | A | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(100): Show | 107 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.535-128A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945756 | ||||||
chr14:72945779 | G | A | 1 | a0002c0004t0006g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535-105G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945779 | ||||||
chr14:72946031 | C | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0098 | 2 | HG02602.hp1 HG04204.hp2 |
splice_region_variant&intron_variant | LOW | c.678+4C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946031 | ||||||
chr14:72946031 | C | T | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.678+4C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946031 | ||||||
chr14:72946056 | G | A | 3 | a0002c0004t0006g0305a0002c0004t0006g0314a0002c0004t0006g0315 | 3 | HG00423.hp1 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.678+29G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946056 | ||||||
chr14:72946072 | GGGTAGTT | G | 43 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(40): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.678+48_678+54delTA others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 72946072 | |||||
chr14:72946227 | C | CA | 9 | a0001c0001t0001g0136a0001c0001t0002g0018a0001c0001t0002g0039others(6): Show | 9 | HG01175.hp1 HG01891.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.678+218dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 72946227 | |||||
chr14:72946227 | CAAAAAAA others(1): Show |
C | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+211_678+218del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 72946227 | |||||
chr14:72946265 | C | T | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0012c0013t0012g0333 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.678+238C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946265 | ||||||
chr14:72946562 | G | A | 2 | a0002c0004t0007g0111a0002c0004t0007g0217 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.678+535G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946562 | ||||||
chr14:72946573 | A | G | 1 | a0002c0004t0007g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.678+546A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946573 | ||||||
chr14:72946660 | G | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.679-482G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946660 | ||||||
chr14:72946667 | G | A | 1 | a0012c0013t0012g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.679-475G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946667 | ||||||
chr14:72946820 | T | C | 2 | a0002c0004t0006g0224a0002c0004t0006g0225 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.679-322T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946820 | ||||||
chr14:72947060 | G | A | 3 | a0001c0002t0001g0221a0001c0002t0004g0381a0001c0002t0004g0382 | 3 | HG01891.hp2 HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.679-82G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72947060 | ||||||
chr14:72947122 | G | A | 23 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(20): Show | 23 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.679-20G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72947122 | ||||||
chr14:72947217 | T | G | 2 | a0001c0002t0001g0350a0001c0002t0001g0359 | 2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.728+26T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947217 | ||||||
chr14:72947252 | T | C | 1 | a0001c0003t0003g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.728+61T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947252 | ||||||
chr14:72947257 | G | C | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.728+66G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947257 | ||||||
chr14:72947438 | G | T | 1 | a0001c0001t0010g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.728+247G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947438 | ||||||
chr14:72947526 | C | G | 1 | a0001c0003t0003g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.728+335C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947526 | ||||||
chr14:72947592 | G | A | 1 | a0001c0003t0008g0334 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728+401G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947592 | ||||||
chr14:72947608 | A | G | 238 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(235): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.728+417A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947608 | ||||||
chr14:72947613 | A | G | 286 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(283): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.728+422A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947613 | ||||||
chr14:72947729 | G | A | 2 | a0001c0002t0001g0200a0001c0002t0004g0294 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.728+538G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947729 | ||||||
chr14:72947810 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.728+619C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947810 | ||||||
chr14:72947839 | A | G | 1 | a0001c0001t0004g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.728+648A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947839 | ||||||
chr14:72947853 | G | T | 1 | a0001c0001t0004g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.728+662G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947853 | ||||||
chr14:72947878 | G | A | 1 | a0001c0001t0004g0329 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.728+687G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947878 | ||||||
chr14:72947904 | G | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.728+713G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947904 | ||||||
chr14:72947939 | A | G | 192 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(189): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.728+748A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947939 | ||||||
chr14:72948076 | G | C | 1 | a0007c0019t0008g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+885G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948076 | ||||||
chr14:72948119 | A | T | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0012c0013t0012g0333 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.728+928A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948119 | ||||||
chr14:72948187 | G | T | 89 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(86): Show | 90 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.728+996G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948187 | ||||||
chr14:72948188 | G | T | 10 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0201others(7): Show | 10 | HG02071.hp2 HG02080.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.728+997G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948188 | ||||||
chr14:72948357 | T | C | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.728+1166T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948357 | ||||||
chr14:72948525 | G | A | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.728+1334G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948525 | ||||||
chr14:72948819 | T | A | 1 | a0002c0004t0007g0139 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.728+1628T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948819 | ||||||
chr14:72948838 | G | A | 6 | a0003c0005t0002g0055a0003c0005t0002g0058a0003c0005t0002g0072others(3): Show | 6 | NA18944.hp2 NA18971.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+1647G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948838 | ||||||
chr14:72948955 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.728+1764T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948955 | ||||||
chr14:72949109 | T | C | 286 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(283): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.728+1918T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949109 | ||||||
chr14:72949119 | G | C | 1 | a0012c0013t0012g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.728+1928G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949119 | ||||||
chr14:72949145 | C | T | 5 | a0001c0001t0002g0086a0001c0001t0002g0092a0001c0001t0002g0095others(2): Show | 5 | HG00140.hp2 HG01496.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+1954C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949145 | ||||||
chr14:72949156 | G | A | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.728+1965G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949156 | ||||||
chr14:72949221 | G | T | 5 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(2): Show | 6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+2030G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949221 | ||||||
chr14:72949366 | G | A | 1 | a0001c0001t0004g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.728+2175G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949366 | ||||||
chr14:72949378 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.728+2187C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949378 | ||||||
chr14:72949416 | A | G | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.728+2225A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949416 | ||||||
chr14:72949426 | A | G | 1 | a0001c0002t0001g0110 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.728+2235A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949426 | ||||||
chr14:72950052 | A | G | 1 | a0002c0004t0006g0314 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.729-1746A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950052 | ||||||
chr14:72950243 | C | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.729-1555C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950243 | ||||||
chr14:72950399 | G | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.729-1399G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950399 | ||||||
chr14:72950599 | G | C | 1 | a0001c0002t0004g0296 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.729-1199G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950599 | ||||||
chr14:72950614 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.729-1184C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950614 | ||||||
chr14:72950684 | G | C | 2 | a0001c0001t0005g0034a0001c0001t0005g0231 | 2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.729-1114G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950684 | ||||||
chr14:72950795 | A | C | 1 | a0001c0002t0001g0359 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.729-1003A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950795 | ||||||
chr14:72950810 | GT | G | 282 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(279): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.729-979delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 72950810 | |||||
chr14:72950830 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.729-968T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950830 | ||||||
chr14:72950858 | T | A | 1 | a0001c0003t0003g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.729-940T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950858 | ||||||
chr14:72950958 | C | T | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.729-840C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950958 | ||||||
chr14:72950972 | T | G | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729-826T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950972 | ||||||
chr14:72950983 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.729-815A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950983 | ||||||
chr14:72951036 | G | A | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.729-762G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951036 | ||||||
chr14:72951089 | T | C | 1 | a0009c0012t0001g0360 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.729-709T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951089 | ||||||
chr14:72951155 | A | G | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.729-643A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951155 | ||||||
chr14:72951214 | C | G | 1 | a0001c0001t0004g0289 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.729-584C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951214 | ||||||
chr14:72951269 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.729-529C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951269 | ||||||
chr14:72951295 | T | C | 1 | a0001c0001t0004g0290 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.729-503T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951295 | ||||||
chr14:72951377 | C | T | 5 | a0001c0007t0008g0280a0001c0007t0008g0342a0001c0007t0008g0343others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-421C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951377 | ||||||
chr14:72951387 | G | A | 43 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(40): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.729-411G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951387 | ||||||
chr14:72951492 | T | C | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.729-306T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951492 | ||||||
chr14:72951669 | T | C | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0012c0013t0012g0333 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.729-129T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951669 | ||||||
chr14:72951715 | G | A | 2 | a0001c0001t0011g0249a0001c0001t0011g0270 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.729-83G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951715 | ||||||
chr14:72951782 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.729-16T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951782 | ||||||
chr14:72952024 | GT | G | 285 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(282): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.808+155delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952024 | |||||
chr14:72952065 | C | T | 1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808+188C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952065 | ||||||
chr14:72952136 | G | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.808+259G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952136 | ||||||
chr14:72952143 | C | T | 2 | a0001c0001t0002g0068a0001c0001t0002g0108 | 2 | NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.808+266C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952143 | ||||||
chr14:72952206 | T | G | 12 | a0001c0001t0003g0250a0001c0003t0008g0262a0001c0003t0008g0263others(9): Show | 12 | HG01074.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.808+329T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952206 | ||||||
chr14:72952229 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.808+352C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952229 | ||||||
chr14:72952303 | C | G | 2 | a0002c0004t0006g0331a0002c0004t0006g0332 | 2 | NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.808+426C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952303 | ||||||
chr14:72952418 | T | C | 1 | a0001c0002t0004g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.808+541T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952418 | ||||||
chr14:72952552 | A | G | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.808+675A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952552 | ||||||
chr14:72952577 | A | T | 2 | a0006c0009t0001g0193a0006c0009t0001g0194 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.808+700A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952577 | ||||||
chr14:72952661 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.808+784G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952661 | ||||||
chr14:72952691 | C | CT | 125 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0195others(122): Show | 130 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.808+834dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952691 | |||||
chr14:72952691 | CT | C | 101 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(98): Show | 105 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.808+834delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952691 | |||||
chr14:72952752 | T | A | 43 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(40): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.808+875T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952752 | ||||||
chr14:72952907 | C | T | 43 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(40): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.808+1030C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952907 | ||||||
chr14:72952928 | C | T | 50 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(47): Show | 52 | HG00323.hp1 HG00423.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.808+1051C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952928 | ||||||
chr14:72952944 | C | T | 1 | a0001c0003t0003g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.808+1067C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952944 | ||||||
chr14:72952972 | T | A | 1 | a0001c0001t0002g0026 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.808+1095T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952972 | ||||||
chr14:72952972 | T | C | 172 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(169): Show | 178 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.808+1095T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952972 | ||||||
chr14:72952982 | A | G | 1 | a0002c0004t0007g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808+1105A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952982 | ||||||
chr14:72952992 | C | CT | 96 | a0001c0001t0001g0136a0001c0001t0001g0191a0001c0001t0001g0197others(93): Show | 100 | HG00408.hp2 HG00544.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.808+1140dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTT | 51 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(48): Show | 52 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.808+1139_808+1140d others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTT | 9 | a0001c0001t0002g0025a0001c0001t0005g0239a0001c0001t0005g0240others(6): Show | 9 | HG00741.hp1 HG01123.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+1138_808+1140d others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTTTT | 20 | a0001c0001t0001g0251a0002c0004t0006g0297a0002c0004t0006g0299others(17): Show | 20 | HG02135.hp1 HG02148.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.808+1136_808+1140d others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTTTTT | 13 | a0002c0004t0006g0009a0002c0004t0006g0298a0002c0004t0006g0304others(10): Show | 14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.808+1135_808+1140d others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTTTTTT others(3): Show |
2 | a0002c0004t0007g0114a0002c0004t0007g0218 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.808+1131_808+1140d others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTTTTTT others(4): Show |
2 | a0002c0004t0007g0111a0002c0004t0007g0222 | 2 | HG01358.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.808+1130_808+1140d others(13): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTTTTTT others(5): Show |
1 | a0002c0004t0007g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.808+1129_808+1140d others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | C | CTTTTTTT others(7): Show |
1 | a0002c0004t0007g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808+1127_808+1140d others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72952992 | CTTT | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 6 | HG01243.hp1 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.808+1138_808+1140d others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | |||||
chr14:72953184 | A | G | 5 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(2): Show | 6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-980A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953184 | ||||||
chr14:72953247 | G | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.809-917G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953247 | ||||||
chr14:72953253 | G | A | 43 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(40): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.809-911G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953253 | ||||||
chr14:72953289 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.809-875C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953289 | ||||||
chr14:72953621 | G | A | 27 | a0001c0001t0005g0006a0001c0001t0005g0034a0001c0001t0005g0231others(24): Show | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.809-543G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953621 | ||||||
chr14:72953709 | T | TA | 22 | a0001c0001t0001g0003a0001c0002t0001g0075a0001c0002t0001g0205others(19): Show | 23 | HG00735.hp2 HG00738.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.809-431dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953709 | T | TAA | 12 | a0001c0002t0001g0074a0001c0002t0001g0201a0002c0004t0006g0299others(9): Show | 12 | HG02055.hp1 HG02071.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-432_809-431dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953709 | T | TAAA | 7 | a0001c0001t0002g0096a0001c0002t0001g0207a0002c0004t0006g0305others(4): Show | 7 | HG00423.hp1 HG02818.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-433_809-431dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953709 | T | TAAAAAAA others(3): Show |
1 | a0001c0002t0001g0024 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.809-440_809-431dup others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953709 | T | TAAAAAAA others(7): Show |
1 | a0002c0004t0007g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.809-444_809-431dup others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953709 | TAA | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0215others(20): Show | 25 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.809-432_809-431del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953709 | TAAAAAAA others(5): Show |
T | 1 | a0011c0011t0004g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.809-442_809-431del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | |||||
chr14:72953721 | AAAAAAAA others(16): Show |
A | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0012c0013t0012g0333 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.809-441_809-419del others(23): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953721 | |||||
chr14:72953725 | AAAAAAAA others(4): Show |
A | 2 | a0006c0009t0001g0193a0006c0009t0001g0194 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.809-437_809-427del others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953725 | |||||
chr14:72953725 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0004g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.809-437_809-423del others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953725 | |||||
chr14:72953726 | A | T | 1 | a0001c0003t0008g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.809-438A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953726 | ||||||
chr14:72953726 | AAAAAAAA others(3): Show |
A | 2 | a0001c0002t0004g0282a0004c0006t0001g0357 | 2 | HG02970.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.809-436_809-427del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953726 | |||||
chr14:72953726 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0004g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.809-436_809-421del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953726 | |||||
chr14:72953728 | A | AAT | 9 | a0001c0001t0001g0125a0001c0001t0001g0340a0001c0001t0004g0292others(6): Show | 9 | HG02129.hp2 HG02155.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-435_809-434ins others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953728 | |||||
chr14:72953728 | A | T | 10 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0336others(7): Show | 10 | HG01975.hp1 HG02109.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-436A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953728 | ||||||
chr14:72953728 | AAAAAATA others(9): Show |
A | 8 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0253others(5): Show | 10 | HG01109.hp1 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-434_809-419del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953728 | |||||
chr14:72953730 | A | AAT | 10 | a0001c0001t0001g0136a0001c0003t0003g0033a0001c0003t0003g0073others(7): Show | 10 | HG02738.hp1 NA18946.hp2 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.809-433_809-432ins others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953730 | |||||
chr14:72953730 | A | AATATATA others(11): Show |
1 | a0001c0001t0002g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.809-433_809-432ins others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953730 | |||||
chr14:72953730 | A | T | 47 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0122others(44): Show | 48 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.809-434A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953730 | ||||||
chr14:72953730 | AAAATATA others(9): Show |
A | 3 | a0001c0001t0004g0252a0001c0001t0004g0256a0001c0001t0004g0329 | 3 | HG02559.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.809-432_809-417del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953730 | |||||
chr14:72953731 | AAAT | A | 6 | a0001c0001t0005g0276a0001c0002t0004g0268a0001c0002t0004g0371others(3): Show | 6 | HG01496.hp1 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-431_809-429del others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953731 | |||||
chr14:72953731 | AAATATAT others(8): Show |
A | 2 | a0001c0001t0011g0249a0001c0001t0011g0270 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.809-431_809-417del others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953731 | |||||
chr14:72953732 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0099a0001c0007t0008g0342 | 2 | HG02004.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0374 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(25): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(3): Show |
3 | a0001c0002t0001g0202a0001c0002t0001g0204a0001c0002t0001g0350 | 3 | HG00558.hp2 HG02135.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0181 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0002g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(21): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(3): Show |
1 | a0001c0002t0001g0321 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0098a0001c0002t0001g0359 | 2 | HG02602.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0002g0368a0001c0007t0008g0345 | 2 | HG00735.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(15): Show |
1 | a0001c0007t0008g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(22): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAA others(17): Show |
1 | a0001c0007t0008g0343 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(24): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAT others(8): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0088a0001c0001t0002g0107 | 3 | NA18946.hp1 NA18950.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAT others(10): Show |
3 | a0001c0001t0002g0045a0001c0001t0002g0087a0001c0001t0002g0369 | 3 | HG00558.hp1 HG00642.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAT others(12): Show |
2 | a0001c0001t0009g0281a0001c0007t0008g0344 | 2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAAAT others(16): Show |
1 | a0001c0001t0002g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(23): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAATA others(3): Show |
2 | a0001c0002t0001g0010a0001c0002t0001g0325 | 3 | NA18971.hp1 NA18988.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAAATA others(13): Show |
1 | a0001c0001t0002g0175 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAATAT others(8): Show |
2 | a0001c0002t0001g0056a0001c0002t0004g0382 | 2 | HG03486.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAAAATAT others(12): Show |
1 | a0001c0001t0002g0022 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAATATAT others(4): Show |
2 | a0001c0002t0001g0126a0001c0002t0004g0381 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | AAATATAT others(10): Show |
5 | a0001c0001t0002g0021a0001c0001t0002g0100a0001c0001t0002g0182others(2): Show | 5 | HG02027.hp1 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-431_809-430ins others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0127 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.809-432_809-431ins others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953732 | ||||||
chr14:72953732 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0102 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.809-432_809-431ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953732 | ||||||
chr14:72953732 | A | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0047others(90): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.809-432A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953732 | ||||||
chr14:72953732 | AATAT | A | 12 | a0001c0001t0005g0034a0001c0001t0005g0231a0001c0001t0005g0235others(9): Show | 12 | HG00544.hp1 HG00741.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-404_809-401del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953732 | AATATAT | A | 14 | a0001c0001t0002g0028a0001c0001t0002g0049a0001c0001t0002g0050others(11): Show | 14 | HG01071.hp1 HG01361.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-406_809-401del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | |||||
chr14:72953733 | ATAT | A | 3 | a0001c0002t0004g0319a0001c0002t0004g0378a0001c0002t0004g0379 | 3 | HG02895.hp1 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.809-430_809-428del others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953733 | ||||||
chr14:72953733 | ATATAT | A | 6 | a0001c0001t0002g0065a0001c0001t0005g0232a0001c0001t0005g0338others(3): Show | 6 | HG00099.hp1 HG01175.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-430_809-426del others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953733 | ||||||
chr14:72953733 | ATATATAT | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(58): Show | 66 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.809-430_809-424del others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953733 | ||||||
chr14:72953734 | T | A | 56 | a0001c0001t0002g0096a0001c0002t0001g0074a0001c0002t0001g0075others(53): Show | 57 | HG00099.hp2 HG00423.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.809-430T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953734 | ||||||
chr14:72953736 | T | A | 37 | a0001c0001t0002g0094a0001c0002t0001g0074a0001c0002t0001g0075others(34): Show | 37 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.809-428T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953736 | ||||||
chr14:72953738 | T | A | 12 | a0001c0001t0002g0094a0001c0002t0001g0074a0001c0002t0001g0075others(9): Show | 12 | HG01070.hp1 HG01928.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-426T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953738 | ||||||
chr14:72953740 | T | A | 14 | a0001c0001t0002g0028a0001c0001t0002g0049a0001c0001t0002g0050others(11): Show | 14 | HG01071.hp1 HG01175.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-424T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953740 | ||||||
chr14:72953742 | T | A | 63 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(60): Show | 67 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.809-422T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953742 | ||||||
chr14:72953744 | T | A | 12 | a0001c0001t0002g0093a0001c0001t0002g0210a0001c0002t0001g0090others(9): Show | 12 | HG00323.hp2 HG01069.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.809-420T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953744 | ||||||
chr14:72953746 | T | A | 4 | a0001c0002t0001g0228a0001c0002t0001g0351a0001c0002t0001g0363others(1): Show | 4 | HG00323.hp2 HG01106.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-418T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953746 | ||||||
chr14:72953755 | ATATATAT others(5): Show |
A | 2 | a0001c0002t0001g0353a0001c0002t0001g0361 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.809-408_809-397del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953755 | ||||||
chr14:72953757 | ATATATAG others(3): Show |
A | 7 | a0001c0002t0001g0110a0001c0002t0001g0230a0001c0002t0001g0348others(4): Show | 7 | HG00099.hp2 HG00741.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-406_809-397del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953757 | ||||||
chr14:72953762 | T | A | 2 | a0001c0002t0004g0376a0001c0002t0004g0380 | 2 | HG01496.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.809-402T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953762 | ||||||
chr14:72953763 | A | AT | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0056others(17): Show | 21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-401_809-400ins others(1): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | ||||||
chr14:72953763 | A | ATATATAT others(6): Show |
1 | a0001c0003t0008g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.809-401_809-400ins others(13): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | ||||||
chr14:72953763 | A | G | 35 | a0001c0001t0003g0250a0001c0001t0005g0006a0001c0001t0005g0034others(32): Show | 36 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.809-401A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | ||||||
chr14:72953763 | AG | A | 6 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0054others(3): Show | 6 | HG01123.hp1 HG02647.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-400delG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | ||||||
chr14:72953764 | G | A | 42 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0056others(39): Show | 43 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.809-400G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953764 | ||||||
chr14:72953764 | G | T | 15 | a0001c0002t0001g0057a0001c0002t0001g0074a0001c0002t0001g0075others(12): Show | 15 | HG01891.hp2 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.809-400G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953764 | ||||||
chr14:72953765 | T | A | 15 | a0001c0002t0001g0057a0001c0002t0001g0074a0001c0002t0001g0075others(12): Show | 15 | HG01891.hp2 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.809-399T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953765 | ||||||
chr14:72953766 | T | A | 28 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(25): Show | 29 | HG00558.hp2 HG01123.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.809-398T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953766 | ||||||
chr14:72953767 | T | A | 15 | a0001c0002t0001g0057a0001c0002t0001g0074a0001c0002t0001g0075others(12): Show | 15 | HG01891.hp2 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.809-397T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953767 | ||||||
chr14:72953768 | A | ATGG | 3 | a0001c0003t0008g0262a0001c0003t0008g0263a0001c0003t0008g0264 | 3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.809-395_809-394ins others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953768 | |||||
chr14:72953770 | T | A | 25 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(22): Show | 26 | HG00558.hp2 HG01123.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.809-394T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953770 | ||||||
chr14:72953774 | T | A | 24 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(21): Show | 25 | HG00558.hp2 HG01123.hp1 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.809-390T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953774 | ||||||
chr14:72953777 | T | TA | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-387_809-386ins others(1): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953777 | ||||||
chr14:72953778 | T | A | 4 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(1): Show | 4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-386T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953778 | ||||||
chr14:72953778 | TTATTTG | T | 4 | a0001c0001t0001g0284a0001c0001t0004g0289a0001c0001t0004g0292others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-384_809-379del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | |||||
chr14:72953778 | TTATTTGT others(1): Show |
T | 3 | a0001c0001t0004g0283a0001c0001t0004g0285a0001c0001t0004g0288 | 3 | HG01243.hp2 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.809-384_809-377del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | |||||
chr14:72953778 | TTATTTGT others(3): Show |
T | 7 | a0001c0001t0001g0016a0001c0001t0001g0216a0001c0001t0002g0064others(4): Show | 7 | HG00738.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-384_809-375del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | |||||
chr14:72953778 | TTATTTGT others(5): Show |
T | 9 | a0001c0001t0002g0084a0001c0002t0001g0351a0001c0002t0001g0363others(6): Show | 9 | HG00323.hp2 HG01361.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-384_809-373del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | |||||
chr14:72953778 | TTATTTGT others(7): Show |
T | 13 | a0001c0002t0001g0228a0001c0002t0001g0229a0001c0002t0001g0322others(10): Show | 13 | HG01069.hp1 HG01106.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.809-384_809-371del others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | |||||
chr14:72953778 | TTATTTGT others(9): Show |
T | 41 | a0001c0002t0001g0090a0002c0004t0006g0009a0002c0004t0006g0224others(38): Show | 42 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.809-384_809-369del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | |||||
chr14:72953779 | T | A | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-385T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953779 | ||||||
chr14:72953780 | A | AATT | 3 | a0001c0002t0001g0054a0001c0002t0001g0356a0001c0002t0001g0372 | 3 | HG01123.hp1 HG03834.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.809-384_809-383ins others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953780 | ||||||
chr14:72953780 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0003g0250 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.809-383_809-382ins others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953780 | |||||
chr14:72953780 | A | G | 2 | a0001c0003t0003g0013a0001c0003t0003g0014 | 2 | HG00642.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.809-384A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953780 | ||||||
chr14:72953780 | ATTTGTGT others(3): Show |
A | 1 | a0001c0003t0008g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.809-382_809-373del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953780 | |||||
chr14:72953782 | T | A | 4 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(1): Show | 4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-382T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953782 | ||||||
chr14:72953782 | T | G | 5 | a0001c0001t0001g0197a0001c0001t0003g0250a0001c0003t0003g0013others(2): Show | 5 | HG00642.hp1 HG01074.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-382T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953782 | ||||||
chr14:72953782 | T | TTG | 16 | a0001c0001t0004g0007a0001c0001t0004g0253a0001c0003t0003g0005others(13): Show | 18 | HG00140.hp1 HG01433.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.809-336_809-335dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | T | TTGTG | 19 | a0001c0003t0003g0033a0001c0003t0003g0073a0001c0003t0003g0077others(16): Show | 19 | HG00423.hp2 HG02015.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.809-338_809-335dup others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTG | T | 25 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0134others(22): Show | 26 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.809-336_809-335del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTGTG | T | 27 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0063others(24): Show | 28 | HG00099.hp1 HG00741.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.809-338_809-335del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTGTGTG | T | 97 | a0001c0001t0001g0117a0001c0001t0001g0191a0001c0001t0002g0001others(94): Show | 101 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.809-340_809-335del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTGTGTGT others(1): Show |
T | 19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0121others(16): Show | 21 | HG00323.hp1 HG00733.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-342_809-335del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTGTGTGT others(3): Show |
T | 18 | a0001c0001t0001g0196a0001c0001t0001g0199a0001c0001t0001g0215others(15): Show | 18 | HG00099.hp2 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.809-344_809-335del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTGTGTGT others(5): Show |
T | 12 | a0001c0001t0005g0231a0001c0002t0001g0057a0001c0002t0001g0074others(9): Show | 12 | HG00544.hp1 HG02015.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.809-346_809-335del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953782 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.809-348_809-335del others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | |||||
chr14:72953784 | G | A | 23 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(20): Show | 24 | HG02135.hp2 HG02165.hp2 HG02976.hp1 others(21): Show |
intron_variant | MODIFIER | c.809-380G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953784 | ||||||
chr14:72953784 | G | T | 4 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(1): Show | 4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-380G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953784 | ||||||
chr14:72953786 | G | A | 5 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(2): Show | 5 | HG00558.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-378G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953786 | ||||||
chr14:72953786 | G | T | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-378G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953786 | ||||||
chr14:72953788 | G | A | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-376G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953788 | ||||||
chr14:72953788 | G | T | 5 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(2): Show | 5 | HG00558.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-376G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953788 | ||||||
chr14:72953790 | G | A | 5 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(2): Show | 5 | HG00558.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-374G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953790 | ||||||
chr14:72953790 | G | T | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-374G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953790 | ||||||
chr14:72953792 | G | A | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-372G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953792 | ||||||
chr14:72953792 | G | T | 4 | a0001c0002t0001g0054a0001c0002t0001g0204a0001c0002t0001g0356others(1): Show | 4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-372G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953792 | ||||||
chr14:72953794 | G | A | 1 | a0001c0002t0001g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.809-370G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953794 | ||||||
chr14:72953794 | G | T | 20 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(17): Show | 21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-370G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953794 | ||||||
chr14:72953796 | G | T | 1 | a0001c0002t0001g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.809-368G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953796 | ||||||
chr14:72953800 | GTGTGTGT others(23): Show |
G | 1 | a0002c0004t0006g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.809-362_809-333del others(30): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953800 | |||||
chr14:72953808 | G | A | 2 | a0002c0004t0006g0331a0002c0004t0006g0332 | 2 | NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.809-356G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953808 | ||||||
chr14:72953812 | G | A | 41 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(38): Show | 42 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.809-352G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953812 | ||||||
chr14:72953814 | GTGTGTGT others(9): Show |
G | 1 | a0001c0003t0003g0156 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.809-348_809-333del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953814 | |||||
chr14:72953818 | GTGTGTGT others(5): Show |
G | 5 | a0001c0003t0003g0227a0001c0007t0008g0342a0001c0007t0008g0343others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-344_809-333del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953818 | |||||
chr14:72953819 | T | A | 1 | a0001c0001t0004g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.809-345T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953819 | ||||||
chr14:72953820 | G | A | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.809-344G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953820 | ||||||
chr14:72953826 | G | A | 175 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(172): Show | 181 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.809-338G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953826 | ||||||
chr14:72953826 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0136 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.809-335_809-334ins others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953826 | |||||
chr14:72953828 | G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0251 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.809-336G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953828 | ||||||
chr14:72953830 | A | G | 4 | a0001c0001t0001g0284a0001c0003t0003g0154a0001c0003t0008g0269others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-334A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953830 | ||||||
chr14:72953934 | G | A | 69 | a0001c0002t0001g0010a0001c0002t0001g0019a0001c0002t0001g0023others(66): Show | 70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.809-230G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953934 | ||||||
chr14:72954025 | C | A | 1 | a0001c0001t0002g0088 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.809-139C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72954025 | ||||||
chr14:72954307 | C | T | 1 | a0001c0015t0003g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.907+45C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/13 | chr14 | 72954307 | ||||||
chr14:72954353 | A | G | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.908-33A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/13 | chr14 | 72954353 | ||||||
chr14:72954381 | G | A | 1 | a0001c0001t0004g0329 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.908-5G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/13 | chr14 | 72954381 | ||||||
chr14:72954554 | ACTC | A | 104 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(101): Show | 108 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1005+75_1005+77del others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 72954554 | |||||
chr14:72954576 | A | C | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1005+93A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72954576 | ||||||
chr14:72954643 | G | A | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005+160G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72954643 | ||||||
chr14:72955035 | C | T | 1 | a0001c0003t0003g0157 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1006-488C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955035 | ||||||
chr14:72955110 | C | CA | 22 | a0001c0001t0001g0136a0001c0001t0002g0088a0001c0001t0002g0101others(19): Show | 24 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-398dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 72955110 | |||||
chr14:72955110 | C | CAAAAA | 43 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(40): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1006-402_1006-398d others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 72955110 | |||||
chr14:72955126 | T | C | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006-397T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955126 | ||||||
chr14:72955171 | G | A | 1 | a0001c0001t0005g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1006-352G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955171 | ||||||
chr14:72955191 | G | T | 44 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(41): Show | 45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-332G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955191 | ||||||
chr14:72955204 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1006-319T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955204 | ||||||
chr14:72955258 | C | G | 374 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0047others(371): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1006-265C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955258 | ||||||
chr14:72955277 | G | C | 6 | a0001c0001t0003g0250a0001c0007t0008g0280a0001c0007t0008g0342others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-246G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955277 | ||||||
chr14:72955734 | G | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1179+38G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955734 | ||||||
chr14:72955831 | AGGCCCTG others(3): Show |
A | 1 | a0001c0002t0001g0323 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1179+138_1179+147d others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955831 | |||||
chr14:72955846 | A | G | 1 | a0001c0001t0004g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1179+150A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955846 | ||||||
chr14:72955854 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1179+158G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955854 | ||||||
chr14:72955914 | C | CT | 42 | a0001c0001t0001g0003a0001c0002t0001g0221a0001c0002t0001g0323others(39): Show | 44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1179+244dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | C | CTT | 12 | a0001c0007t0008g0344a0002c0004t0006g0297a0002c0004t0006g0303others(9): Show | 13 | HG01168.hp2 HG01261.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1179+243_1179+244d others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | C | CTTT | 6 | a0001c0001t0001g0137a0001c0001t0001g0337a0001c0001t0011g0249others(3): Show | 6 | HG00323.hp1 HG00544.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+242_1179+244d others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | C | CTTTT | 6 | a0001c0001t0001g0078a0001c0001t0001g0134a0001c0001t0001g0138others(3): Show | 6 | HG02735.hp1 HG03579.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+241_1179+244d others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | C | CTTTTT | 7 | a0001c0001t0001g0135a0001c0001t0001g0189a0001c0001t0001g0192others(4): Show | 7 | HG00408.hp1 HG02056.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+240_1179+244d others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | C | CTTTTTTT others(10): Show |
1 | a0013c0018t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1179+228_1179+244d others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | CT | C | 162 | a0001c0001t0001g0216a0001c0001t0001g0284a0001c0001t0002g0018others(159): Show | 167 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1179+244delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | CTT | C | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0020others(96): Show | 103 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1179+243_1179+244d others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955914 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1179+233_1179+244d others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | |||||
chr14:72955944 | A | G | 2 | a0001c0001t0002g0079a0001c0001t0002g0101 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1179+248A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955944 | ||||||
chr14:72955946 | G | A | 38 | a0002c0004t0006g0009a0002c0004t0006g0224a0002c0004t0006g0225others(35): Show | 39 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1179+250G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955946 | ||||||
chr14:72955975 | T | G | 1 | a0001c0001t0005g0272 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1179+279T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955975 | ||||||
chr14:72956264 | A | G | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0012c0013t0012g0333 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1180-122A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72956264 | ||||||
chr14:72956679 | G | A | 1 | a0001c0003t0003g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1294+179G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956679 | ||||||
chr14:72956867 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1294+367C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956867 | ||||||
chr14:72956885 | G | A | 4 | a0001c0002t0001g0228a0001c0002t0001g0229a0001c0002t0001g0230others(1): Show | 4 | HG01106.hp2 HG01257.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+385G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956885 | ||||||
chr14:72956952 | C | T | 7 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(4): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1294+452C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956952 | ||||||
chr14:72957104 | C | G | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1294+604C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957104 | ||||||
chr14:72957119 | G | A | 122 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(119): Show | 126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1294+619G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957119 | ||||||
chr14:72957143 | C | T | 3 | a0001c0003t0003g0005a0001c0003t0003g0166a0001c0003t0003g0167 | 4 | HG00140.hp1 HG01433.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294+643C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957143 | ||||||
chr14:72957161 | G | A | 6 | a0001c0001t0004g0370a0001c0002t0001g0126a0001c0002t0001g0127others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1294+661G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957161 | ||||||
chr14:72957163 | T | C | 9 | a0001c0002t0004g0268a0001c0002t0004g0282a0001c0002t0004g0319others(6): Show | 9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1294+663T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957163 | ||||||
chr14:72957211 | AAAAT | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1294+727_1294+730d others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 72957211 | |||||
chr14:72957399 | A | G | 13 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0252others(10): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1294+899A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957399 | ||||||
chr14:72957584 | C | G | 5 | a0004c0006t0001g0011a0004c0006t0001g0213a0004c0006t0001g0214others(2): Show | 6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-1028C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957584 | ||||||
chr14:72957701 | G | A | 27 | a0001c0001t0005g0006a0001c0001t0005g0034a0001c0001t0005g0231others(24): Show | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1295-911G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957701 | ||||||
chr14:72957875 | T | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0041 | 4 | NA19003.hp1 NA19007.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1295-737T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957875 | ||||||
chr14:72958106 | C | T | 164 | a0001c0001t0003g0250a0001c0001t0004g0370a0001c0001t0005g0006others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1295-506C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958106 | ||||||
chr14:72958112 | C | CA | 24 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0048others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1295-486dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 72958112 | |||||
chr14:72958112 | CA | C | 8 | a0001c0001t0002g0116a0001c0001t0005g0236a0001c0001t0005g0271others(5): Show | 8 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-486delA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 72958112 | |||||
chr14:72958247 | C | T | 382 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(379): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1295-365C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958247 | ||||||
chr14:72958345 | C | T | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1295-267C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958345 | ||||||
chr14:72958516 | C | A | 1 | a0001c0001t0009g0208 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1295-96C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958516 | ||||||
chr14:72958607 | C | T | 123 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(120): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
splice_region_variant&intron_variant | LOW | c.1295-5C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958607 |