geneid | 80067 |
---|---|
ensemblid | ENSG00000115827.14 |
hgncid | 25784 |
symbol | DCAF17 |
name | DDB1 and CUL4 associated factor 17 |
refseq_nuc | NM_025000.4 |
refseq_prot | NP_079276.2 |
ensembl_nuc | ENST00000375255.8 |
ensembl_prot | ENSP00000364404.3 |
mane_status | MANE Select |
chr | chr2 |
start | 171434226 |
end | 171485052 |
strand | + |
ver | v1.2 |
region | chr2:171434226-171485052 |
region5000 | chr2:171429226-171490052 |
regionname0 | DCAF17_chr2_171434226_171485052 |
regionname5000 | DCAF17_chr2_171429226_171490052 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 520 | 338 | 84 | 58 | 153 | 12 | 29 | 122 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0002 | 0/0 | 520 | 20 | 5 | 1 | 11 | 0 | 3 | 6 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0003 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0004 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1563 | 209 | 47 | 42 | 89 | 11 | 18 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0002 | 0/0 | 1563 | 93 | 14 | 15 | 53 | 1 | 10 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0003 | 0/0 | 1563 | 20 | 5 | 1 | 11 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0004 | 0/0 | 1563 | 14 | 14 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0005 | 0/0 | 1563 | 13 | 7 | 1 | 5 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0006 | 0/0 | 1563 | 6 | 0 | 0 | 5 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0007 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0008 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0009 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0010 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
c0011 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4291 | 188 | 29 | 41 | 90 | 11 | 17 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0002 | 0/0 | 4291 | 89 | 13 | 14 | 52 | 1 | 9 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0003 | 0/0 | 4291 | 18 | 3 | 1 | 11 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0004 | 0/0 | 4291 | 13 | 13 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0005 | 1/0 | 4291 | 10 | 9 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0006 | 0/0 | 4291 | 9 | 9 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0007 | 0/0 | 4291 | 7 | 5 | 2 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0008 | 0/0 | 4291 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0009 | 0/0 | 4291 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0010 | 0/0 | 4291 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0011 | 0/0 | 4291 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0012 | 0/0 | 4291 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0013 | 0/0 | 4291 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0014 | 0/1 | 4291 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0015 | 0/0 | 4291 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0016 | 0/0 | 4291 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0017 | 0/0 | 4291 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0018 | 0/0 | 4291 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0019 | 0/0 | 4291 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0020 | 0/0 | 4291 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0021 | 0/0 | 4291 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0022 | 0/0 | 4291 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0023 | 0/0 | 4291 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0024 | 0/0 | 4291 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0025 | 0/0 | 4291 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0026 | 0/0 | 4291 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
t0027 | 0/0 | 4291 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 0 | 0 | 19 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0002 | 0/0 | 8 | 0 | 3 | 2 | 1 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0007 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0038 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1563 | 209 | 47 | 42 | 89 | 11 | 18 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002 | 0/0 | 1563 | 93 | 14 | 15 | 53 | 1 | 10 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0004 | 0/0 | 1563 | 14 | 14 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0005 | 0/0 | 1563 | 13 | 7 | 1 | 5 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0006 | 0/0 | 1563 | 6 | 0 | 0 | 5 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0007 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0009 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0010 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0002c0003 | 0/0 | 1563 | 20 | 5 | 1 | 11 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0003c0008 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0004c0011 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5853 | 182 | 27 | 40 | 87 | 11 | 17 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0005 | 1/0 | 5853 | 10 | 9 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0006 | 0/0 | 5853 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0007 | 0/0 | 5853 | 6 | 5 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0012 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0014 | 0/1 | 5853 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0016 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0018 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0019 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0020 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0021 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0001t0024 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002t0002 | 0/0 | 5853 | 88 | 13 | 14 | 51 | 1 | 9 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002t0015 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002t0023 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002t0025 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002t0026 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0002t0027 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0004t0004 | 0/0 | 5853 | 13 | 13 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0004t0017 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0005t0006 | 0/0 | 5853 | 6 | 6 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0005t0007 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0005t0008 | 0/0 | 5853 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0005t0011 | 0/0 | 5853 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0005t0013 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0006t0001 | 0/0 | 5853 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0006t0009 | 0/0 | 5853 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0006t0022 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0007t0001 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0009t0002 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0001c0010t0001 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0002c0003t0003 | 0/0 | 5853 | 18 | 3 | 1 | 11 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0002c0003t0010 | 0/0 | 5853 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0003c0008t0012 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
a0004c0011t0001 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | copy fasta | chr2 | 171429226 | 171490052 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 3 | 2 | 1 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0005g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0014g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0018g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0019g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0021g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0001t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0015g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0023g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0025g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0026g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0002t0027g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0004t0017g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0006g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0005t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0006t0009g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0006t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0006t0022g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0009t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0001c0010t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0002c0003t0010g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0003c0008t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
a0004c0011t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0025 | EUR | FIN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00408 | hp2 | a0001 | c0005 | t0008 | g0056 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00423 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00558 | hp1 | a0001 | c0005 | t0011 | g0058 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG00741 | hp2 | a0004 | c0011 | t0001 | g0181 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0204 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01081 | hp2 | a0002 | c0003 | t0003 | g0224 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01192 | hp1 | a0001 | c0002 | t0023 | g0025 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01261 | hp1 | a0001 | c0005 | t0007 | g0210 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0081 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01884 | hp2 | a0002 | c0003 | t0010 | g0043 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02027 | hp1 | a0002 | c0003 | t0003 | g0222 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02040 | hp1 | a0001 | c0005 | t0008 | g0055 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02055 | hp1 | a0001 | c0005 | t0006 | g0050 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02056 | hp2 | a0001 | c0006 | t0009 | g0128 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02080 | hp1 | a0002 | c0003 | t0003 | g0042 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02083 | hp2 | a0001 | c0006 | t0022 | g0035 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02129 | hp2 | a0002 | c0003 | t0003 | g0226 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02132 | hp1 | a0002 | c0003 | t0003 | g0223 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02145 | hp2 | a0001 | c0001 | t0021 | g0148 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02155 | hp1 | a0001 | c0006 | t0001 | g0035 | EAS | CDX | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0106 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02602 | hp2 | a0001 | c0002 | t0026 | g0030 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02647 | hp1 | a0001 | c0005 | t0006 | g0023 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02647 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0195 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02717 | hp2 | a0001 | c0005 | t0013 | g0049 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02735 | hp2 | a0001 | c0001 | t0018 | g0236 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02809 | hp2 | a0001 | c0001 | t0024 | g0177 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02818 | hp2 | a0002 | c0003 | t0003 | g0041 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02895 | hp2 | a0001 | c0004 | t0004 | g0040 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02896 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02897 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02970 | hp1 | a0001 | c0004 | t0004 | g0214 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02970 | hp2 | a0001 | c0010 | t0001 | g0200 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02976 | hp1 | a0001 | c0004 | t0004 | g0211 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03098 | hp2 | a0001 | c0005 | t0006 | g0052 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03139 | hp1 | a0002 | c0003 | t0003 | g0041 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03139 | hp2 | a0002 | c0003 | t0010 | g0043 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03209 | hp2 | a0001 | c0004 | t0004 | g0209 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03453 | hp1 | a0001 | c0007 | t0001 | g0124 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03453 | hp2 | a0001 | c0005 | t0006 | g0048 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03486 | hp2 | a0001 | c0004 | t0004 | g0135 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03540 | hp1 | a0001 | c0004 | t0004 | g0213 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03540 | hp2 | a0001 | c0005 | t0006 | g0023 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03654 | hp2 | a0002 | c0003 | t0003 | g0227 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03704 | hp2 | a0002 | c0003 | t0003 | g0225 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03927 | hp2 | a0001 | c0006 | t0009 | g0123 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0086 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04204 | hp2 | a0002 | c0003 | t0003 | g0042 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0114 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CHB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18906 | hp1 | a0003 | c0008 | t0012 | g0159 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18906 | hp2 | a0001 | c0004 | t0004 | g0215 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18941 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18942 | hp1 | a0001 | c0005 | t0008 | g0059 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18957 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18959 | hp1 | a0002 | c0003 | t0003 | g0062 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18959 | hp2 | a0001 | c0001 | t0016 | g0169 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18963 | hp1 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18969 | hp2 | a0002 | c0003 | t0003 | g0266 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18983 | hp1 | a0001 | c0006 | t0001 | g0125 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18992 | hp2 | a0001 | c0002 | t0015 | g0031 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19005 | hp2 | a0002 | c0003 | t0003 | g0228 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19006 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19009 | hp2 | a0001 | c0006 | t0001 | g0126 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19030 | hp2 | a0001 | c0001 | t0012 | g0158 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19063 | hp2 | a0001 | c0005 | t0011 | g0057 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19066 | hp1 | a0001 | c0009 | t0002 | g0140 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19080 | hp2 | a0001 | c0002 | t0027 | g0094 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA19240 | hp2 | a0001 | c0004 | t0004 | g0208 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA20129 | hp1 | a0001 | c0004 | t0004 | g0040 | AFR | ASW | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01123 | hp1 | a0001 | c0001 | t0019 | g0257 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02486 | hp2 | a0001 | c0002 | t0025 | g0110 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03471 | hp1 | a0001 | c0004 | t0017 | g0212 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0097 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA20300 | hp1 | a0001 | c0004 | t0004 | g0207 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA20300 | hp2 | a0001 | c0005 | t0006 | g0051 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA21309 | hp1 | a0002 | c0003 | t0003 | g0229 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0014 | g0038 | REF | REF | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0242 | REF | REF | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171435165
|
A | G | 1 | a0004 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.209A>G | p.Asn70Ser | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/14 | 561/5853 | 209/1563 | 70/520 | chr2 | 171435165 | ||
chr2:171453141
|
T | A | 1 | a0002 | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
missense_variant | MODERATE | c.555T>A | p.His185Gln | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/14 | 907/5853 | 555/1563 | 185/520 | chr2 | 171453141 | ||
chr2:171468965
|
G | A | 1 | a0003 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.916G>A | p.Val306Ile | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/14 | 1268/5853 | 916/1563 | 306/520 | chr2 | 171468965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171435106
|
C | T | 4 | a0001c0002a0001c0004a0001c0005others(1): Show | 140 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
synonymous_variant | LOW | c.150C>T | p.Val50Val | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/14 | 502/5853 | 150/1563 | 50/520 | chr2 | 171435106 | ||
chr2:171458431
|
T | C | 1 | a0001c0007 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.792T>C | p.Thr264Thr | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/14 | 1144/5853 | 792/1563 | 264/520 | chr2 | 171458431 | ||
chr2:171468904
|
C | T | 1 | a0001c0010 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.855C>T | p.Leu285Leu | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/14 | 1207/5853 | 855/1563 | 285/520 | chr2 | 171468904 | ||
chr2:171468988
|
G | A | 1 | a0001c0004 | 14 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(11): Show |
synonymous_variant | LOW | c.939G>A | p.Gln313Gln | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/14 | 1291/5853 | 939/1563 | 313/520 | chr2 | 171468988 | ||
chr2:171473883
|
A | G | 2 | a0001c0002a0001c0009 | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
synonymous_variant | LOW | c.999A>G | p.Gln333Gln | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/14 | 1351/5853 | 999/1563 | 333/520 | chr2 | 171473883 | ||
chr2:171480091
|
T | C | 1 | a0001c0006 | 6 | HG02056.hp2 HG02083.hp2 HG02155.hp1 others(3): Show |
synonymous_variant | LOW | c.1320T>C | p.Ala440Ala | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/14 | 1672/5853 | 1320/1563 | 440/520 | chr2 | 171480091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171434467
|
G | T | 2 | a0001c0002t0026a0001c0002t0027 | 2 | HG02602.hp2 NA19080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-111G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 111 | chr2 | 171434467 | |||||
chr2:171434483
|
C | T | 1 | a0001c0002t0025 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 95 | chr2 | 171434483 | |||||
chr2:171434514
|
A | G | 1 | a0001c0001t0024 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 64 | chr2 | 171434514 | |||||
chr2:171434519
|
G | A | 1 | a0001c0005t0013 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 59 | chr2 | 171434519 | |||||
chr2:171481129
|
T | C | 1 | a0001c0006t0009 | 2 | HG02056.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*15T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 15 | chr2 | 171481129 | |||||
chr2:171481302
|
T | A | 1 | a0001c0001t0014 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 188 | chr2 | 171481302 | |||||
chr2:171481464
|
G | A | 2 | a0002c0003t0003a0002c0003t0010 | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 350 | chr2 | 171481464 | |||||
chr2:171481492
|
T | C | 2 | a0001c0005t0008a0001c0005t0011 | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 378 | chr2 | 171481492 | |||||
chr2:171481568
|
A | C | 1 | a0001c0002t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 454 | chr2 | 171481568 | |||||
chr2:171481644
|
A | G | 1 | a0002c0003t0010 | 2 | HG01884.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*530A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 530 | chr2 | 171481644 | |||||
chr2:171481684
|
G | A | 6 | a0001c0002t0002a0001c0002t0015a0001c0002t0023others(3): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 570 | chr2 | 171481684 | |||||
chr2:171481790
|
T | G | 6 | a0001c0002t0002a0001c0002t0015a0001c0002t0023others(3): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*676T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 676 | chr2 | 171481790 | |||||
chr2:171481791
|
C | A | 2 | a0001c0001t0012a0003c0008t0012 | 2 | NA18906.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 677 | chr2 | 171481791 | |||||
chr2:171481810
|
A | G | 1 | a0001c0006t0022 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 696 | chr2 | 171481810 | |||||
chr2:171482119
|
A | G | 3 | a0001c0001t0006a0001c0005t0006a0001c0005t0013 | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1005A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 1005 | chr2 | 171482119 | |||||
chr2:171482148
|
G | A | 2 | a0001c0005t0008a0001c0005t0011 | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 1034 | chr2 | 171482148 | |||||
chr2:171482635
|
A | G | 2 | a0001c0005t0008a0001c0005t0011 | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1521A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 1521 | chr2 | 171482635 | |||||
chr2:171483297
|
C | G | 5 | a0001c0001t0006a0001c0005t0006a0001c0005t0008others(2): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2183C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2183 | chr2 | 171483297 | |||||
chr2:171483312
|
T | G | 1 | a0001c0001t0016 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2198 | chr2 | 171483312 | |||||
chr2:171483454
|
C | T | 34 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(31): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*2340C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2340 | chr2 | 171483454 | |||||
chr2:171483462
|
G | A | 2 | a0001c0001t0007a0001c0005t0007 | 7 | HG01074.hp2 HG01261.hp1 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2348G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2348 | chr2 | 171483462 | |||||
chr2:171483494
|
A | G | 1 | a0001c0001t0021 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2380A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2380 | chr2 | 171483494 | |||||
chr2:171483539
|
T | A | 6 | a0001c0002t0002a0001c0002t0015a0001c0002t0023others(3): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2425T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2425 | chr2 | 171483539 | |||||
chr2:171483587
|
G | A | 2 | a0001c0004t0004a0001c0004t0017 | 14 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2473 | chr2 | 171483587 | |||||
chr2:171483889
|
G | T | 2 | a0002c0003t0003a0002c0003t0010 | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2775G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2775 | chr2 | 171483889 | |||||
chr2:171483909
|
T | C | 13 | a0001c0001t0006a0001c0002t0002a0001c0002t0015others(10): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2795T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2795 | chr2 | 171483909 | |||||
chr2:171484061
|
A | C | 1 | a0001c0001t0020 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2947A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2947 | chr2 | 171484061 | |||||
chr2:171484085
|
A | G | 1 | a0001c0001t0019 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2971A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2971 | chr2 | 171484085 | |||||
chr2:171484090
|
A | G | 1 | a0001c0005t0008 | 3 | HG00408.hp2 HG02040.hp1 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2976A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2976 | chr2 | 171484090 | |||||
chr2:171484226
|
C | G | 6 | a0001c0002t0002a0001c0002t0015a0001c0002t0023others(3): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3112C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3112 | chr2 | 171484226 | |||||
chr2:171484242
|
C | G | 1 | a0001c0001t0018 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3128C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3128 | chr2 | 171484242 | |||||
chr2:171484505
|
T | C | 1 | a0001c0002t0015 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3391T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3391 | chr2 | 171484505 | |||||
chr2:171484656
|
A | C | 1 | a0001c0004t0017 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3542 | chr2 | 171484656 | |||||
chr2:171484817
|
A | G | 6 | a0001c0002t0002a0001c0002t0015a0001c0002t0023others(3): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3703A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3703 | chr2 | 171484817 | |||||
chr2:171484826
|
A | G | 3 | a0001c0001t0006a0001c0005t0006a0001c0005t0013 | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3712A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3712 | chr2 | 171484826 | |||||
chr2:171484943
|
G | A | 5 | a0001c0001t0006a0001c0005t0006a0001c0005t0008others(2): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3829G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3829 | chr2 | 171484943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:171434838
|
C | G | 3 | a0002c0003t0003g0022a0002c0003t0003g0265a0002c0003t0003g0266 | 5 | HG00423.hp2 NA18941.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+135C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/13 | chr2 | 171434838 | ||||||
chr2:171435034
|
T | G | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-49T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/13 | chr2 | 171435034 | ||||||
chr2:171435068
|
C | A | 3 | a0001c0002t0002g0024a0001c0002t0002g0053a0001c0002t0002g0054 | 4 | HG01258.hp1 HG01433.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-15C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/13 | chr2 | 171435068 | ||||||
chr2:171435293
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.230+107A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435293 | ||||||
chr2:171435547
|
C | CT | 23 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 28 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.230+377dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171435547 | |||||
chr2:171435547
|
CT | C | 89 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0005g0063others(86): Show | 111 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.230+377delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171435547 | |||||
chr2:171435639
|
C | T | 2 | a0001c0005t0006g0023a0001c0005t0006g0052 | 3 | HG02647.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.230+453C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435639 | ||||||
chr2:171435705
|
A | G | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.230+519A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435705 | ||||||
chr2:171435752
|
A | G | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.230+566A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435752 | ||||||
chr2:171436030
|
T | G | 3 | a0001c0001t0005g0034a0001c0001t0005g0117a0001c0001t0005g0118 | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+844T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436030 | ||||||
chr2:171436209
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.230+1023G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436209 | ||||||
chr2:171436215
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(259): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.230+1029G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436215 | ||||||
chr2:171436234
|
T | C | 4 | a0001c0001t0005g0063a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+1048T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436234 | ||||||
chr2:171436327
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.230+1141A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436327 | ||||||
chr2:171436633
|
A | AT | 16 | a0001c0001t0001g0221a0001c0001t0001g0237a0002c0003t0003g0022others(13): Show | 21 | HG00423.hp2 HG01081.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.230+1464dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436633 | |||||
chr2:171436633
|
AT | A | 110 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(107): Show | 133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.230+1464delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436633 | |||||
chr2:171436774
|
A | AT | 74 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(71): Show | 92 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.230+1605dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436774 | |||||
chr2:171436774
|
AT | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0120others(4): Show | 7 | HG01168.hp1 HG02897.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.230+1605delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436774 | |||||
chr2:171436868
|
G | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.230+1682G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436868 | ||||||
chr2:171436957
|
A | G | 79 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(76): Show | 98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+1771A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436957 | ||||||
chr2:171437027
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.230+1841G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437027 | ||||||
chr2:171437033
|
CA | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0262 | 3 | HG00280.hp1 HG02300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.230+1850delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171437033 | |||||
chr2:171437055
|
T | C | 2 | a0002c0003t0003g0222a0002c0003t0003g0223 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.230+1869T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437055 | ||||||
chr2:171437282
|
C | A | 1 | a0001c0002t0002g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.230+2096C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437282 | ||||||
chr2:171437350
|
T | G | 79 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(76): Show | 98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+2164T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437350 | ||||||
chr2:171437395
|
C | T | 27 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0025others(24): Show | 34 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.230+2209C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437395 | ||||||
chr2:171437396
|
A | G | 79 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(76): Show | 98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+2210A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437396 | ||||||
chr2:171437533
|
T | C | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.230+2347T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437533 | ||||||
chr2:171437946
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0018g0236 | 4 | HG02735.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+2760A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437946 | ||||||
chr2:171437958
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.230+2772C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437958 | ||||||
chr2:171438052
|
G | A | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.230+2866G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438052 | ||||||
chr2:171438170
|
TTA | T | 4 | a0001c0005t0006g0023a0001c0005t0006g0050a0001c0005t0006g0051others(1): Show | 5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.230+2986_230+2987d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171438170 | |||||
chr2:171438278
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.230+3092T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438278 | ||||||
chr2:171438282
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 120 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.230+3096G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438282 | ||||||
chr2:171438303
|
G | A | 2 | a0002c0003t0003g0224a0002c0003t0003g0225 | 2 | HG01081.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.230+3117G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438303 | ||||||
chr2:171438363
|
AGTTGACT | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.230+3179_230+3185d others(9): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171438363 | |||||
chr2:171438501
|
C | T | 1 | a0001c0002t0002g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.230+3315C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438501 | ||||||
chr2:171438510
|
C | T | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.230+3324C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438510 | ||||||
chr2:171438594
|
T | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG00140.hp2 HG01175.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+3408T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438594 | ||||||
chr2:171438746
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.230+3560T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438746 | ||||||
chr2:171438801
|
A | G | 79 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(76): Show | 98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+3615A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438801 | ||||||
chr2:171438849
|
A | G | 1 | a0001c0002t0002g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.230+3663A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438849 | ||||||
chr2:171438909
|
T | TAGAGATA others(96): Show |
75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.230+3742_230+3743i others(105): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171438909 | |||||
chr2:171438920
|
G | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.230+3734G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438920 | ||||||
chr2:171439031
|
G | A | 101 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(98): Show | 126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.230+3845G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439031 | ||||||
chr2:171439076
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.230+3890A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439076 | ||||||
chr2:171439089
|
C | A | 1 | a0001c0005t0006g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.230+3903C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439089 | ||||||
chr2:171439170
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.230+3984C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439170 | ||||||
chr2:171439232
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.230+4046C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439232 | ||||||
chr2:171439270
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.230+4084C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439270 | ||||||
chr2:171439284
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.230+4098A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439284 | ||||||
chr2:171439310
|
A | G | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.230+4124A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439310 | ||||||
chr2:171439369
|
G | C | 86 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(83): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.231-4154G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439369 | ||||||
chr2:171439485
|
T | C | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.231-4038T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439485 | ||||||
chr2:171439511
|
C | CT | 15 | a0001c0001t0001g0143a0001c0001t0001g0205a0001c0001t0001g0206others(12): Show | 18 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.231-3991dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171439511 | |||||
chr2:171439511
|
CT | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(87): Show | 131 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.231-3991delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171439511 | |||||
chr2:171439576
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.231-3947G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439576 | ||||||
chr2:171439696
|
G | A | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.231-3827G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439696 | ||||||
chr2:171439718
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 7 | HG00741.hp1 HG01361.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.231-3805A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439718 | ||||||
chr2:171439722
|
G | C | 1 | a0002c0003t0003g0224 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.231-3801G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439722 | ||||||
chr2:171439728
|
C | G | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.231-3795C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439728 | ||||||
chr2:171439843
|
G | C | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3680G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439843 | ||||||
chr2:171439907
|
G | C | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3616G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439907 | ||||||
chr2:171440006
|
A | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-3517A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440006 | ||||||
chr2:171440226
|
A | G | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-3297A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440226 | ||||||
chr2:171440272
|
A | G | 101 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(98): Show | 126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.231-3251A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440272 | ||||||
chr2:171440343
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3180A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440343 | ||||||
chr2:171440401
|
C | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3122C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440401 | ||||||
chr2:171440443
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3080C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440443 | ||||||
chr2:171440517
|
C | T | 4 | a0001c0005t0006g0023a0001c0005t0006g0050a0001c0005t0006g0051others(1): Show | 5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-3006C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440517 | ||||||
chr2:171440522
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-3001C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440522 | ||||||
chr2:171440567
|
G | C | 101 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(98): Show | 126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.231-2956G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440567 | ||||||
chr2:171440598
|
A | G | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-2925A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440598 | ||||||
chr2:171440923
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0189 | 4 | HG02155.hp2 NA18977.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-2600C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440923 | ||||||
chr2:171440924
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-2599G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440924 | ||||||
chr2:171441004
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.231-2519A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441004 | ||||||
chr2:171441086
|
G | A | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.231-2437G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441086 | ||||||
chr2:171441091
|
G | A | 2 | a0001c0005t0006g0048a0001c0005t0013g0049 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.231-2432G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441091 | ||||||
chr2:171441450
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.231-2073C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441450 | ||||||
chr2:171441480
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.231-2043C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441480 | ||||||
chr2:171441539
|
A | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-1984A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441539 | ||||||
chr2:171441557
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0205 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.231-1966G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441557 | ||||||
chr2:171441632
|
A | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG01074.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.231-1891A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441632 | ||||||
chr2:171441767
|
G | A | 1 | a0001c0002t0002g0067 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.231-1756G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441767 | ||||||
chr2:171441897
|
T | TGGGGGGG others(13): Show |
1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1626_231-1625i others(22): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441897 | ||||||
chr2:171441916
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1607C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441916 | ||||||
chr2:171441941
|
TTATCACA others(5): Show |
T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1581_231-1570d others(14): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441941 | ||||||
chr2:171441954
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1569G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441954 | ||||||
chr2:171441956
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1567A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441956 | ||||||
chr2:171442026
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1497A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442026 | ||||||
chr2:171442028
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1495T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442028 | ||||||
chr2:171442031
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1492A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442031 | ||||||
chr2:171442152
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0039others(17): Show | 26 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.231-1371C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442152 | ||||||
chr2:171442175
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1348C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442175 | ||||||
chr2:171442185
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1338A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442185 | ||||||
chr2:171442188
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1335T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442188 | ||||||
chr2:171442189
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1334C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442189 | ||||||
chr2:171442191
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1332A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442191 | ||||||
chr2:171442192
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1331A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442192 | ||||||
chr2:171442211
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1312C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442211 | ||||||
chr2:171442212
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1311A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442212 | ||||||
chr2:171442220
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1303A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442220 | ||||||
chr2:171442222
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1301T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442222 | ||||||
chr2:171442251
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1272A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442251 | ||||||
chr2:171442252
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1271A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442252 | ||||||
chr2:171442253
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1270A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442253 | ||||||
chr2:171442258
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1265A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442258 | ||||||
chr2:171442261
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1262T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442261 | ||||||
chr2:171442267
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1256A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442267 | ||||||
chr2:171442268
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1255A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442268 | ||||||
chr2:171442271
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1252A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442271 | ||||||
chr2:171442272
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1251A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442272 | ||||||
chr2:171442275
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1248G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442275 | ||||||
chr2:171442284
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1239C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442284 | ||||||
chr2:171442285
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1238G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442285 | ||||||
chr2:171442296
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1227C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442296 | ||||||
chr2:171442296
|
C | T | 2 | a0001c0004t0004g0214a0001c0004t0004g0215 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-1227C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442296 | ||||||
chr2:171442373
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1150A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442373 | ||||||
chr2:171442382
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1141C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442382 | ||||||
chr2:171442476
|
A | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.231-1047A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442476 | ||||||
chr2:171442478
|
C | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.231-1045C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442478 | ||||||
chr2:171442563
|
C | CA | 15 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(12): Show | 15 | HG00408.hp2 HG00558.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.231-940dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171442563 | |||||
chr2:171442563
|
CA | C | 75 | a0001c0001t0001g0004a0001c0001t0001g0134a0001c0001t0001g0247others(72): Show | 97 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.231-940delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171442563 | |||||
chr2:171442740
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-783C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442740 | ||||||
chr2:171443029
|
G | T | 1 | a0001c0004t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.231-494G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443029 | ||||||
chr2:171443251
|
G | A | 1 | a0001c0002t0002g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.231-272G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443251 | ||||||
chr2:171443292
|
T | C | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-231T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443292 | ||||||
chr2:171443347
|
GT | G | 6 | a0001c0001t0005g0063a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-167delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171443347 | |||||
chr2:171443349
|
T | TA | 115 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(112): Show | 143 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.231-174_231-173ins others(1): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443349 | ||||||
chr2:171443831
|
A | AT | 8 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0005t0006g0023others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+226dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171443831 | |||||
chr2:171443831
|
AT | A | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+226delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171443831 | |||||
chr2:171443899
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+286A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171443899 | ||||||
chr2:171443909
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0250a0001c0001t0001g0251others(1): Show | 5 | HG00280.hp1 HG01106.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+296A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171443909 | ||||||
chr2:171444241
|
G | A | 8 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0005t0006g0023others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+628G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444241 | ||||||
chr2:171444354
|
A | G | 1 | a0002c0003t0003g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.321+741A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444354 | ||||||
chr2:171444638
|
A | G | 1 | a0001c0005t0006g0051 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.321+1025A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444638 | ||||||
chr2:171444682
|
G | A | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+1069G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444682 | ||||||
chr2:171444727
|
A | G | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.321+1114A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444727 | ||||||
chr2:171444745
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.321+1132A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444745 | ||||||
chr2:171444749
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.321+1136C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444749 | ||||||
chr2:171444798
|
G | A | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.321+1185G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444798 | ||||||
chr2:171444858
|
T | A | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1245T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444858 | ||||||
chr2:171445132
|
A | AT | 87 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0201others(84): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.321+1531dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171445132 | |||||
chr2:171445325
|
A | C | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+1712A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445325 | ||||||
chr2:171445495
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.321+1882C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445495 | ||||||
chr2:171445557
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0205 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.321+1944C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445557 | ||||||
chr2:171445607
|
C | T | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.321+1994C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445607 | ||||||
chr2:171445692
|
T | C | 1 | a0001c0001t0006g0219 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.321+2079T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445692 | ||||||
chr2:171445808
|
A | G | 114 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(111): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.321+2195A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445808 | ||||||
chr2:171445868
|
A | C | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+2255A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445868 | ||||||
chr2:171445930
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.321+2317G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445930 | ||||||
chr2:171445995
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.321+2382A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445995 | ||||||
chr2:171446256
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.322-2425C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446256 | ||||||
chr2:171446501
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.322-2180A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446501 | ||||||
chr2:171446573
|
T | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-2108T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446573 | ||||||
chr2:171446705
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1976A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446705 | ||||||
chr2:171446767
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1914A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446767 | ||||||
chr2:171446927
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0184 | 2 | HG01069.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.322-1754G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446927 | ||||||
chr2:171446940
|
C | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.322-1741C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446940 | ||||||
chr2:171446946
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.322-1735T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446946 | ||||||
chr2:171446951
|
G | T | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-1730G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446951 | ||||||
chr2:171446962
|
A | C | 1 | a0001c0002t0002g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.322-1719A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446962 | ||||||
chr2:171446973
|
C | G | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-1708C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446973 | ||||||
chr2:171446980
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.322-1701A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446980 | ||||||
chr2:171447045
|
A | G | 39 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0024others(36): Show | 47 | HG00597.hp2 HG01109.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.322-1636A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447045 | ||||||
chr2:171447127
|
G | A | 6 | a0001c0005t0006g0023a0001c0005t0006g0048a0001c0005t0006g0050others(3): Show | 7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-1554G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447127 | ||||||
chr2:171447190
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1491C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447190 | ||||||
chr2:171447199
|
A | C | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1482A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447199 | ||||||
chr2:171447322
|
A | C | 2 | a0001c0004t0004g0006a0001c0004t0017g0212 | 4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-1359A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447322 | ||||||
chr2:171447401
|
G | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 20 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.322-1280G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447401 | ||||||
chr2:171447454
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.322-1227G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447454 | ||||||
chr2:171447583
|
C | T | 2 | a0001c0002t0002g0028a0001c0002t0002g0111 | 3 | NA18991.hp2 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.322-1098C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447583 | ||||||
chr2:171447675
|
C | T | 132 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(129): Show | 163 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.322-1006C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447675 | ||||||
chr2:171447686
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-995G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447686 | ||||||
chr2:171447830
|
C | T | 2 | a0001c0005t0006g0023a0001c0005t0006g0052 | 3 | HG02647.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.322-851C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447830 | ||||||
chr2:171447854
|
ACTTCCAC others(10): Show |
A | 1 | a0001c0002t0002g0070 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.322-824_322-808del others(17): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171447854 | |||||
chr2:171448016
|
G | T | 1 | a0002c0003t0003g0223 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.322-665G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448016 | ||||||
chr2:171448082
|
C | T | 29 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0025others(26): Show | 37 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.322-599C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448082 | ||||||
chr2:171448085
|
G | A | 4 | a0001c0005t0006g0023a0001c0005t0006g0050a0001c0005t0006g0051others(1): Show | 5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.322-596G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448085 | ||||||
chr2:171448120
|
G | A | 1 | a0001c0002t0002g0071 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.322-561G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448120 | ||||||
chr2:171448154
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-527C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448154 | ||||||
chr2:171448177
|
G | T | 2 | a0001c0001t0001g0119a0004c0011t0001g0181 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.322-504G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448177 | ||||||
chr2:171448178
|
C | T | 2 | a0001c0001t0001g0119a0004c0011t0001g0181 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.322-503C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448178 | ||||||
chr2:171448429
|
T | TAAC | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-252_322-251ins others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448429 | ||||||
chr2:171448582
|
T | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-99T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448582 | ||||||
chr2:171448585
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.322-96G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448585 | ||||||
chr2:171448608
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.322-73C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448608 | ||||||
chr2:171448665
|
C | CT | 71 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(68): Show | 89 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.322-15dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171448665 | |||||
chr2:171448667
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-14C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448667 | ||||||
chr2:171448932
|
A | G | 5 | a0001c0001t0001g0196a0001c0001t0007g0017a0001c0001t0007g0197others(2): Show | 8 | HG01074.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.458+115A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171448932 | ||||||
chr2:171449151
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.458+334G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449151 | ||||||
chr2:171449177
|
T | A | 1 | a0001c0004t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.458+360T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449177 | ||||||
chr2:171449271
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.458+454G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449271 | ||||||
chr2:171449295
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.458+478A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449295 | ||||||
chr2:171449392
|
A | G | 1 | a0001c0004t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.459-487A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449392 | ||||||
chr2:171449506
|
T | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.459-373T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449506 | ||||||
chr2:171449638
|
G | A | 77 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0002t0002g0003others(74): Show | 96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.459-241G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449638 | ||||||
chr2:171449689
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(24): Show | 41 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.459-190A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449689 | ||||||
chr2:171449973
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0232others(2): Show | 8 | HG02083.hp1 NA18964.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+16C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171449973 | ||||||
chr2:171450153
|
T | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG00140.hp2 HG01175.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+196T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450153 | ||||||
chr2:171450180
|
C | T | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.537+223C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450180 | ||||||
chr2:171450209
|
C | A | 1 | a0001c0006t0009g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.537+252C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450209 | ||||||
chr2:171450641
|
G | A | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.537+684G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450641 | ||||||
chr2:171450701
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.537+744T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450701 | ||||||
chr2:171450739
|
C | G | 1 | a0004c0011t0001g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.537+782C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450739 | ||||||
chr2:171450748
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.537+791G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450748 | ||||||
chr2:171450808
|
G | A | 103 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(100): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.537+851G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450808 | ||||||
chr2:171450875
|
C | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0119others(14): Show | 20 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.537+918C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450875 | ||||||
chr2:171450900
|
G | A | 86 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(83): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.537+943G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450900 | ||||||
chr2:171450938
|
G | A | 1 | a0001c0010t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.537+981G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450938 | ||||||
chr2:171450964
|
T | C | 8 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0005t0006g0023others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+1007T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450964 | ||||||
chr2:171451074
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+1117A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451074 | ||||||
chr2:171451085
|
T | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(75): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.537+1128T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451085 | ||||||
chr2:171451212
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.537+1255G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451212 | ||||||
chr2:171451395
|
C | CTCTCTTA others(1): Show |
5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+1440_537+1447d others(10): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 171451395 | |||||
chr2:171451418
|
T | C | 1 | a0001c0001t0005g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.537+1461T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451418 | ||||||
chr2:171451533
|
T | C | 3 | a0001c0001t0005g0034a0001c0001t0005g0117a0001c0001t0005g0118 | 4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+1576T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451533 | ||||||
chr2:171451649
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.538-1475C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451649 | ||||||
chr2:171451715
|
A | G | 1 | a0001c0002t0002g0109 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.538-1409A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451715 | ||||||
chr2:171451759
|
A | G | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.538-1365A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451759 | ||||||
chr2:171451853
|
A | G | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.538-1271A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451853 | ||||||
chr2:171451881
|
G | A | 1 | a0001c0004t0017g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.538-1243G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451881 | ||||||
chr2:171451927
|
A | G | 1 | a0001c0002t0002g0084 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.538-1197A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451927 | ||||||
chr2:171452100
|
G | C | 103 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0002t0002g0003others(100): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.538-1024G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452100 | ||||||
chr2:171452289
|
G | C | 1 | a0001c0002t0002g0093 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.538-835G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452289 | ||||||
chr2:171452380
|
C | T | 2 | a0001c0006t0009g0123a0001c0006t0009g0128 | 2 | HG02056.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.538-744C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452380 | ||||||
chr2:171452524
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538-600G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452524 | ||||||
chr2:171452567
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(79): Show | 123 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.538-557C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452567 | ||||||
chr2:171452571
|
A | G | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.538-553A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452571 | ||||||
chr2:171452643
|
G | A | 2 | a0001c0004t0004g0207a0001c0004t0004g0213 | 2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.538-481G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452643 | ||||||
chr2:171452996
|
T | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.538-128T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452996 | ||||||
chr2:171453391
|
T | G | 1 | a0002c0003t0003g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.627+178T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171453391 | ||||||
chr2:171453436
|
G | A | 1 | a0002c0003t0003g0041 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.627+223G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171453436 | ||||||
chr2:171453704
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0174 | 4 | NA18947.hp2 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+491C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171453704 | ||||||
chr2:171454036
|
T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.627+823T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454036 | ||||||
chr2:171454245
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 286 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.627+1032C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454245 | ||||||
chr2:171454345
|
C | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+1132C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454345 | ||||||
chr2:171454371
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.627+1158G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454371 | ||||||
chr2:171454430
|
G | A | 76 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(73): Show | 95 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.627+1217G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454430 | ||||||
chr2:171454473
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.627+1260A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454473 | ||||||
chr2:171454635
|
A | G | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+1422A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454635 | ||||||
chr2:171454688
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.627+1475G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454688 | ||||||
chr2:171454765
|
T | C | 1 | a0001c0002t0002g0029 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.627+1552T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454765 | ||||||
chr2:171454882
|
CA | C | 13 | a0001c0001t0006g0243a0001c0002t0002g0113a0001c0005t0006g0023others(10): Show | 14 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+1682delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 171454882 | |||||
chr2:171454902
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.627+1689A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454902 | ||||||
chr2:171454993
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.627+1780T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454993 | ||||||
chr2:171455059
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.627+1846G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455059 | ||||||
chr2:171455130
|
CCCACCCT | C | 102 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(99): Show | 127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.627+1934_627+1940d others(9): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 171455130 | |||||
chr2:171455161
|
C | A | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.627+1948C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455161 | ||||||
chr2:171455390
|
G | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+2177G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455390 | ||||||
chr2:171455432
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.627+2219G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455432 | ||||||
chr2:171455535
|
G | A | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+2322G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455535 | ||||||
chr2:171455597
|
C | T | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-2374C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455597 | ||||||
chr2:171455785
|
T | C | 3 | a0001c0001t0007g0017a0001c0001t0007g0195a0001c0001t0007g0204 | 5 | HG01074.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-2186T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455785 | ||||||
chr2:171456739
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-1232A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456739 | ||||||
chr2:171456742
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0205 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-1229A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456742 | ||||||
chr2:171456763
|
A | G | 1 | a0001c0004t0004g0211 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.628-1208A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456763 | ||||||
chr2:171456788
|
G | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.628-1183G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456788 | ||||||
chr2:171456797
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-1174A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456797 | ||||||
chr2:171456831
|
G | C | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-1140G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456831 | ||||||
chr2:171456880
|
A | G | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-1091A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456880 | ||||||
chr2:171457056
|
C | G | 6 | a0001c0001t0001g0249a0001c0001t0001g0256a0001c0001t0001g0258others(3): Show | 6 | HG00642.hp1 HG01109.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-915C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457056 | ||||||
chr2:171457172
|
G | A | 1 | a0001c0002t0027g0094 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.628-799G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457172 | ||||||
chr2:171457214
|
G | T | 6 | a0001c0001t0001g0249a0001c0001t0001g0256a0001c0001t0001g0258others(3): Show | 6 | HG00642.hp1 HG01109.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-757G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457214 | ||||||
chr2:171457384
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(17): Show | 23 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-587T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457384 | ||||||
chr2:171457403
|
C | G | 114 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(111): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.628-568C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457403 | ||||||
chr2:171457523
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.628-448G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457523 | ||||||
chr2:171457603
|
A | C | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0019g0257 | 3 | HG01109.hp2 HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.628-368A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457603 | ||||||
chr2:171457636
|
C | T | 1 | a0001c0002t0025g0110 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.628-335C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457636 | ||||||
chr2:171457744
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.628-227G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457744 | ||||||
chr2:171457934
|
T | G | 3 | a0001c0004t0004g0207a0001c0004t0004g0208a0001c0004t0004g0213 | 3 | HG03540.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.628-37T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457934 | ||||||
chr2:171458134
|
A | AT | 12 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0119others(9): Show | 15 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.732+70dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 171458134 | |||||
chr2:171458134
|
AT | A | 79 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(76): Show | 99 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.732+70delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 171458134 | |||||
chr2:171458595
|
A | G | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+118A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458595 | ||||||
chr2:171458603
|
A | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.838+126A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458603 | ||||||
chr2:171458701
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+224C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458701 | ||||||
chr2:171458772
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.838+295A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458772 | ||||||
chr2:171458830
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0205 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.838+353C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458830 | ||||||
chr2:171458958
|
A | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+481A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458958 | ||||||
chr2:171459052
|
G | A | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+575G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459052 | ||||||
chr2:171459080
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+603C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459080 | ||||||
chr2:171459122
|
C | A | 1 | a0001c0002t0002g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.838+645C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459122 | ||||||
chr2:171459152
|
A | T | 2 | a0001c0002t0002g0009a0001c0002t0002g0108 | 4 | NA18952.hp2 NA18962.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+675A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459152 | ||||||
chr2:171459258
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.838+781G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459258 | ||||||
chr2:171459399
|
C | G | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.838+922C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459399 | ||||||
chr2:171459419
|
A | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+942A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459419 | ||||||
chr2:171459566
|
C | T | 7 | a0001c0004t0004g0040a0001c0004t0004g0135a0001c0004t0004g0209others(4): Show | 8 | HG01261.hp1 HG02895.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.838+1089C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459566 | ||||||
chr2:171459592
|
T | A | 2 | a0001c0004t0004g0006a0001c0004t0017g0212 | 4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+1115T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459592 | ||||||
chr2:171459664
|
G | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1187G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459664 | ||||||
chr2:171459755
|
A | G | 2 | a0001c0002t0002g0088a0001c0002t0002g0107 | 2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.838+1278A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459755 | ||||||
chr2:171459852
|
C | T | 1 | a0001c0005t0011g0057 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.838+1375C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459852 | ||||||
chr2:171459980
|
T | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1503T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459980 | ||||||
chr2:171460121
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1644G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460121 | ||||||
chr2:171460162
|
A | C | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+1685A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460162 | ||||||
chr2:171460270
|
C | A | 1 | a0001c0002t0002g0074 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.838+1793C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460270 | ||||||
chr2:171460275
|
A | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1798A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460275 | ||||||
chr2:171460290
|
T | C | 1 | a0001c0002t0002g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.838+1813T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460290 | ||||||
chr2:171460301
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+1824C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460301 | ||||||
chr2:171460310
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1833G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460310 | ||||||
chr2:171460322
|
CA | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0173others(7): Show | 10 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.838+1864delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171460322 | |||||
chr2:171460322
|
CAA | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1863_838+1864d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171460322 | |||||
chr2:171460476
|
G | T | 1 | a0001c0001t0005g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.838+1999G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460476 | ||||||
chr2:171460513
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.838+2036C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460513 | ||||||
chr2:171460543
|
A | ATTATTAT others(17): Show |
1 | a0001c0002t0002g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.838+2066_838+2067i others(26): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | ATTATTAT others(14): Show |
6 | a0001c0002t0002g0007a0001c0002t0002g0064a0001c0002t0002g0069others(3): Show | 8 | HG03669.hp2 HG03688.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(23): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | ATTATTAT others(11): Show |
24 | a0001c0002t0002g0003a0001c0002t0002g0025a0001c0002t0002g0026others(21): Show | 30 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(20): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | ATTATTAT others(5): Show |
3 | a0001c0002t0002g0030a0001c0002t0002g0090a0001c0002t0026g0030 | 3 | HG02109.hp1 HG02602.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.838+2066_838+2067i others(14): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | ATTATTAT others(2): Show |
37 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(34): Show | 47 | HG00597.hp2 HG01109.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(11): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | ATTATTT | 9 | a0001c0002t0002g0032a0001c0002t0002g0087a0001c0002t0002g0105others(6): Show | 10 | HG00408.hp2 HG00558.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(8): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | ATTT | 2 | a0001c0001t0001g0036a0001c0007t0001g0124 | 3 | HG01891.hp2 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.838+2066_838+2067i others(5): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460543
|
A | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(178): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.838+2066A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | ||||||
chr2:171460574
|
A | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+2097A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460574 | ||||||
chr2:171460622
|
T | C | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+2145T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460622 | ||||||
chr2:171460822
|
C | T | 5 | a0001c0002t0002g0032a0001c0002t0002g0087a0001c0002t0002g0103others(2): Show | 6 | HG01952.hp2 HG01975.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+2345C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460822 | ||||||
chr2:171460946
|
T | A | 1 | a0002c0003t0003g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.838+2469T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460946 | ||||||
chr2:171461122
|
C | A | 1 | a0001c0001t0021g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.838+2645C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461122 | ||||||
chr2:171461202
|
T | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+2725T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461202 | ||||||
chr2:171461352
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.838+2875A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461352 | ||||||
chr2:171461373
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.838+2896G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461373 | ||||||
chr2:171461382
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(28): Show | 53 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.838+2905G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461382 | ||||||
chr2:171461490
|
AAG | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3017_838+3018d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171461490 | |||||
chr2:171461638
|
T | G | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+3161T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461638 | ||||||
chr2:171461650
|
C | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3173C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461650 | ||||||
chr2:171461802
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3325C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461802 | ||||||
chr2:171461803
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.838+3326G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461803 | ||||||
chr2:171461849
|
CT | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.838+3380delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171461849 | |||||
chr2:171462416
|
T | A | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+3939T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462416 | ||||||
chr2:171462447
|
T | C | 2 | a0001c0001t0012g0158a0003c0008t0012g0159 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.838+3970T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462447 | ||||||
chr2:171462466
|
G | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3989G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462466 | ||||||
chr2:171462486
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0162a0001c0001t0001g0217 | 3 | NA19064.hp2 NA19068.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.838+4009C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462486 | ||||||
chr2:171462671
|
C | T | 1 | a0002c0003t0003g0223 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.838+4194C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462671 | ||||||
chr2:171462833
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+4356G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462833 | ||||||
chr2:171462951
|
A | G | 1 | a0001c0002t0002g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.838+4474A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462951 | ||||||
chr2:171463183
|
C | T | 87 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(84): Show | 107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.838+4706C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463183 | ||||||
chr2:171463187
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+4710G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463187 | ||||||
chr2:171463220
|
AT | A | 8 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(5): Show | 9 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+4747delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463220 | |||||
chr2:171463222
|
T | TA | 5 | a0001c0002t0002g0069a0001c0002t0002g0072a0001c0002t0002g0073others(2): Show | 5 | HG02615.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+4745_838+4746i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463222 | ||||||
chr2:171463223
|
T | A | 80 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(77): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.838+4746T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463223 | ||||||
chr2:171463224
|
T | A | 106 | a0001c0001t0001g0045a0001c0001t0001g0149a0001c0001t0001g0234others(103): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.838+4747T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463224 | ||||||
chr2:171463225
|
A | T | 10 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(7): Show | 13 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.838+4748A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463225 | ||||||
chr2:171463301
|
T | TA | 7 | a0001c0001t0001g0122a0001c0001t0005g0117a0001c0005t0008g0055others(4): Show | 7 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.838+4840dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463301 | |||||
chr2:171463503
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.838+5026A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463503 | ||||||
chr2:171463715
|
G | T | 2 | a0001c0002t0002g0031a0001c0002t0015g0031 | 2 | NA18950.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.839-5173G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463715 | ||||||
chr2:171463779
|
TGCTTTTA others(9): Show |
T | 2 | a0001c0001t0001g0047a0001c0001t0001g0262 | 3 | HG00280.hp1 HG02300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.839-5105_839-5090d others(18): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463779 | |||||
chr2:171463810
|
A | AGAAATAA others(2916): Show |
1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.839-5064_839-5063i others(2925): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463810 | |||||
chr2:171463990
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.839-4898T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463990 | ||||||
chr2:171464321
|
G | A | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.839-4567G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171464321 | ||||||
chr2:171464808
|
TAACTC | T | 3 | a0001c0002t0002g0072a0001c0002t0002g0073a0001c0002t0002g0078 | 3 | HG02615.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.839-4078_839-4074d others(7): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171464808 | |||||
chr2:171464852
|
C | CTA | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.839-4026_839-4025d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171464852 | |||||
chr2:171465059
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.839-3829G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465059 | ||||||
chr2:171465102
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.839-3786G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465102 | ||||||
chr2:171465156
|
C | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02258.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.839-3732C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465156 | ||||||
chr2:171465189
|
C | T | 7 | a0001c0002t0002g0032a0001c0002t0002g0087a0001c0002t0002g0102others(4): Show | 8 | HG01952.hp2 HG01975.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-3699C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465189 | ||||||
chr2:171465204
|
G | GA | 12 | a0001c0001t0001g0150a0001c0001t0001g0176a0001c0001t0001g0199others(9): Show | 12 | HG02027.hp2 HG02055.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.839-3670dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171465204 | |||||
chr2:171465204
|
GA | G | 6 | a0001c0001t0001g0171a0001c0005t0008g0055a0001c0005t0008g0056others(3): Show | 6 | HG00408.hp2 HG00558.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-3670delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171465204 | |||||
chr2:171465311
|
G | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-3577G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465311 | ||||||
chr2:171465325
|
T | C | 5 | a0001c0002t0002g0003a0001c0002t0002g0071a0001c0002t0002g0076others(2): Show | 9 | HG00408.hp1 NA18947.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-3563T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465325 | ||||||
chr2:171465386
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-3502G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465386 | ||||||
chr2:171465477
|
C | T | 1 | a0001c0002t0002g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.839-3411C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465477 | ||||||
chr2:171465584
|
C | G | 1 | a0001c0002t0002g0106 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.839-3304C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465584 | ||||||
chr2:171465626
|
C | A | 4 | a0001c0001t0005g0063a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.839-3262C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465626 | ||||||
chr2:171465648
|
T | A | 1 | a0001c0002t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.839-3240T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465648 | ||||||
chr2:171465683
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.839-3205C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465683 | ||||||
chr2:171465748
|
G | T | 1 | a0001c0002t0002g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.839-3140G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465748 | ||||||
chr2:171465937
|
T | C | 18 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(15): Show | 24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-2951T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465937 | ||||||
chr2:171466023
|
A | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-2865A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466023 | ||||||
chr2:171466031
|
T | A | 1 | a0001c0001t0007g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.839-2857T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466031 | ||||||
chr2:171466304
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-2584G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466304 | ||||||
chr2:171466411
|
A | C | 2 | a0002c0003t0003g0062a0002c0003t0003g0228 | 2 | NA18959.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.839-2477A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466411 | ||||||
chr2:171466414
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(77): Show | 119 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.839-2474G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466414 | ||||||
chr2:171466497
|
G | A | 1 | a0001c0002t0002g0065 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.839-2391G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466497 | ||||||
chr2:171466589
|
G | GAAT | 136 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0045others(133): Show | 168 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.839-2297_839-2295d others(5): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466589 | |||||
chr2:171466592
|
T | G | 1 | a0001c0001t0005g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.839-2296T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466592 | ||||||
chr2:171466687
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-2201C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466687 | ||||||
chr2:171466702
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.839-2186C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466702 | ||||||
chr2:171466715
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.839-2173T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466715 | ||||||
chr2:171466727
|
G | GT | 17 | a0001c0001t0001g0127a0001c0001t0001g0256a0001c0001t0001g0264others(14): Show | 22 | HG00423.hp2 HG00642.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-2146dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466727 | |||||
chr2:171466727
|
GT | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 56 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.839-2146delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466727 | |||||
chr2:171466727
|
GTT | G | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.839-2147_839-2146d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466727 | |||||
chr2:171466731
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.839-2157T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466731 | ||||||
chr2:171466735
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.839-2153T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466735 | ||||||
chr2:171466758
|
A | G | 5 | a0001c0002t0002g0010a0001c0002t0002g0033a0001c0002t0002g0092others(2): Show | 8 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-2130A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466758 | ||||||
chr2:171466807
|
C | G | 2 | a0001c0002t0002g0033a0001c0002t0002g0092 | 3 | HG02615.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.839-2081C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466807 | ||||||
chr2:171466951
|
T | TG | 87 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(84): Show | 107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.839-1937_839-1936i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466951 | ||||||
chr2:171466957
|
T | C | 1 | a0001c0002t0002g0103 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.839-1931T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466957 | ||||||
chr2:171466969
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.839-1919G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466969 | ||||||
chr2:171467034
|
A | G | 87 | a0001c0001t0006g0243a0001c0002t0002g0003a0001c0002t0002g0007others(84): Show | 107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.839-1854A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467034 | ||||||
chr2:171467082
|
T | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-1806T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467082 | ||||||
chr2:171467200
|
T | G | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-1688T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467200 | ||||||
chr2:171467221
|
TA | T | 18 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(15): Show | 24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-1657delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467221 | |||||
chr2:171467273
|
A | G | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG01074.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-1615A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467273 | ||||||
chr2:171467283
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.839-1605A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467283 | ||||||
chr2:171467334
|
CTATT | C | 12 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(9): Show | 13 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.839-1550_839-1547d others(6): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467334 | |||||
chr2:171467411
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-1477C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467411 | ||||||
chr2:171467455
|
G | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-1433G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467455 | ||||||
chr2:171467595
|
G | T | 1 | a0002c0003t0010g0043 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.839-1293G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467595 | ||||||
chr2:171467613
|
T | TGTAATAC others(12): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0120a0001c0001t0001g0134others(1): Show | 5 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-1273_839-1255d others(21): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467613 | |||||
chr2:171467727
|
C | CA | 10 | a0001c0001t0001g0129a0001c0001t0001g0146a0001c0001t0001g0163others(7): Show | 10 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.839-1134dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | |||||
chr2:171467727
|
C | CG | 3 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0192 | 3 | HG00140.hp2 HG04228.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.839-1161_839-1160i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467727 | ||||||
chr2:171467727
|
CA | C | 16 | a0001c0001t0001g0038a0001c0001t0001g0061a0001c0001t0001g0134others(13): Show | 19 | HG01169.hp2 HG01255.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.839-1134delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | |||||
chr2:171467727
|
CAA | C | 13 | a0001c0001t0006g0243a0001c0002t0002g0067a0001c0002t0002g0069others(10): Show | 14 | HG02055.hp1 HG02300.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-1135_839-1134d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | |||||
chr2:171467727
|
CAAA | C | 69 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(66): Show | 88 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.839-1136_839-1134d others(5): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | |||||
chr2:171467728
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0119others(9): Show | 15 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.839-1160A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467728 | ||||||
chr2:171467729
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.839-1159A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467729 | ||||||
chr2:171467735
|
A | AC | 18 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(15): Show | 24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-1153_839-1152i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467735 | ||||||
chr2:171467743
|
A | C | 10 | a0001c0001t0006g0243a0001c0002t0002g0093a0001c0002t0002g0100others(7): Show | 11 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.839-1145A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467743 | ||||||
chr2:171467748
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0252 | 2 | HG00140.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.839-1140A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467748 | ||||||
chr2:171467749
|
A | C | 105 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(102): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.839-1139A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467749 | ||||||
chr2:171467824
|
A | G | 2 | a0001c0001t0006g0219a0001c0001t0006g0220 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.839-1064A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467824 | ||||||
chr2:171467910
|
A | G | 2 | a0001c0005t0008g0056a0001c0005t0008g0059 | 2 | HG00408.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.839-978A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467910 | ||||||
chr2:171467988
|
T | A | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-900T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467988 | ||||||
chr2:171467989
|
T | A | 12 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(9): Show | 13 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.839-899T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467989 | ||||||
chr2:171468107
|
C | G | 12 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(9): Show | 15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.839-781C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468107 | ||||||
chr2:171468280
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839-608T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468280 | ||||||
chr2:171468306
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0174a0001c0001t0016g0169 | 5 | NA18947.hp2 NA18959.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-582A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468306 | ||||||
chr2:171468468
|
T | A | 2 | a0001c0005t0006g0048a0001c0005t0013g0049 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-420T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468468 | ||||||
chr2:171468630
|
A | G | 105 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(102): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.839-258A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468630 | ||||||
chr2:171468652
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-236C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468652 | ||||||
chr2:171468702
|
G | C | 1 | a0001c0002t0002g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.839-186G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468702 | ||||||
chr2:171469221
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.981+191C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469221 | ||||||
chr2:171469363
|
T | C | 1 | a0001c0005t0006g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.981+333T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469363 | ||||||
chr2:171469380
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0264 | 4 | NA18946.hp1 NA18950.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+350G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469380 | ||||||
chr2:171469558
|
G | A | 6 | a0001c0002t0002g0025a0001c0002t0002g0067a0001c0002t0002g0068others(3): Show | 6 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+528G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469558 | ||||||
chr2:171469717
|
T | C | 9 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.981+687T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469717 | ||||||
chr2:171469753
|
T | G | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+723T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469753 | ||||||
chr2:171470066
|
T | C | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+1036T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470066 | ||||||
chr2:171470072
|
A | G | 89 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(86): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.981+1042A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470072 | ||||||
chr2:171470235
|
G | A | 1 | a0002c0003t0003g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.981+1205G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470235 | ||||||
chr2:171470390
|
G | A | 9 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.981+1360G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470390 | ||||||
chr2:171470393
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(77): Show | 119 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.981+1363C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470393 | ||||||
chr2:171470397
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0174a0001c0001t0016g0169 | 5 | NA18947.hp2 NA18959.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+1367A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470397 | ||||||
chr2:171470471
|
C | A | 2 | a0002c0003t0003g0224a0002c0003t0003g0225 | 2 | HG01081.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.981+1441C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470471 | ||||||
chr2:171470578
|
C | T | 1 | a0001c0005t0006g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.981+1548C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470578 | ||||||
chr2:171470653
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.981+1623G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470653 | ||||||
chr2:171470829
|
G | A | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.981+1799G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470829 | ||||||
chr2:171470841
|
C | A | 11 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(8): Show | 14 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+1811C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470841 | ||||||
chr2:171470843
|
G | A | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+1813G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470843 | ||||||
chr2:171471274
|
G | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(13): Show | 19 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+2244G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471274 | ||||||
chr2:171471280
|
T | TA | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+2258dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 171471280 | |||||
chr2:171471608
|
G | T | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-2258G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471608 | ||||||
chr2:171471937
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-1929G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471937 | ||||||
chr2:171471939
|
C | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-1927C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471939 | ||||||
chr2:171471940
|
A | G | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-1926A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471940 | ||||||
chr2:171472007
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0155 | 2 | HG02015.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.982-1859C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472007 | ||||||
chr2:171472146
|
A | G | 1 | a0001c0002t0027g0094 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.982-1720A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472146 | ||||||
chr2:171472219
|
G | A | 1 | a0001c0005t0006g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982-1647G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472219 | ||||||
chr2:171472241
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.982-1625A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472241 | ||||||
chr2:171472243
|
G | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.982-1623G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472243 | ||||||
chr2:171472274
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.982-1592G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472274 | ||||||
chr2:171472371
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-1495G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472371 | ||||||
chr2:171472389
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.982-1477C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472389 | ||||||
chr2:171472402
|
C | T | 1 | a0001c0002t0002g0029 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.982-1464C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472402 | ||||||
chr2:171472558
|
C | A | 9 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.982-1308C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472558 | ||||||
chr2:171472692
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(260): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.982-1174T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472692 | ||||||
chr2:171472753
|
G | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.982-1113G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472753 | ||||||
chr2:171472948
|
G | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-918G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472948 | ||||||
chr2:171473077
|
C | G | 1 | a0001c0006t0001g0126 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.982-789C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473077 | ||||||
chr2:171473100
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.982-766T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473100 | ||||||
chr2:171473425
|
C | T | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.982-441C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473425 | ||||||
chr2:171473496
|
A | C | 89 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(86): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.982-370A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473496 | ||||||
chr2:171473565
|
A | AT | 18 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(15): Show | 24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.982-300dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 171473565 | |||||
chr2:171473567
|
C | A | 18 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(15): Show | 24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.982-299C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473567 | ||||||
chr2:171473615
|
T | C | 14 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(11): Show | 15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.982-251T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473615 | ||||||
chr2:171473623
|
TA | T | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-241delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 171473623 | |||||
chr2:171473700
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0263 | 3 | HG02083.hp1 NA18964.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.982-166T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473700 | ||||||
chr2:171473785
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.982-81T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473785 | ||||||
chr2:171473990
|
T | C | 1 | a0001c0001t0018g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1091+15T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171473990 | ||||||
chr2:171474198
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1091+223T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474198 | ||||||
chr2:171474256
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG01192.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1091+281A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474256 | ||||||
chr2:171474447
|
A | G | 1 | a0001c0002t0002g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1091+472A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474447 | ||||||
chr2:171474502
|
A | G | 2 | a0001c0006t0001g0125a0001c0006t0001g0126 | 2 | NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1091+527A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474502 | ||||||
chr2:171474583
|
A | G | 20 | a0001c0001t0001g0045a0001c0001t0001g0247a0001c0001t0001g0252others(17): Show | 26 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1091+608A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474583 | ||||||
chr2:171474721
|
G | A | 7 | a0001c0001t0006g0243a0001c0005t0006g0023a0001c0005t0006g0048others(4): Show | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091+746G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474721 | ||||||
chr2:171474760
|
C | G | 1 | a0001c0005t0006g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1091+785C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474760 | ||||||
chr2:171474828
|
G | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(268): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1091+853G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474828 | ||||||
chr2:171474890
|
C | T | 9 | a0001c0004t0004g0006a0001c0004t0004g0040a0001c0004t0004g0135others(6): Show | 12 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091+915C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474890 | ||||||
chr2:171475201
|
C | T | 1 | a0001c0001t0005g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1091+1226C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475201 | ||||||
chr2:171475256
|
C | T | 1 | a0002c0003t0010g0043 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1091+1281C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475256 | ||||||
chr2:171475410
|
C | G | 1 | a0001c0002t0002g0108 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1091+1435C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475410 | ||||||
chr2:171475410
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+1435C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475410 | ||||||
chr2:171475424
|
A | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0252 | 3 | HG00140.hp1 HG01515.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1092-1436A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475424 | ||||||
chr2:171475458
|
A | G | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1092-1402A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475458 | ||||||
chr2:171475525
|
G | A | 1 | a0002c0003t0003g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1092-1335G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475525 | ||||||
chr2:171475531
|
G | A | 4 | a0001c0001t0005g0063a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-1329G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475531 | ||||||
chr2:171475585
|
T | C | 2 | a0001c0001t0006g0219a0001c0001t0006g0220 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1092-1275T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475585 | ||||||
chr2:171475660
|
G | A | 29 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0025others(26): Show | 37 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1092-1200G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475660 | ||||||
chr2:171475821
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0206 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092-1039A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475821 | ||||||
chr2:171475914
|
G | A | 1 | a0001c0002t0002g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092-946G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475914 | ||||||
chr2:171476019
|
A | G | 1 | a0001c0002t0002g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1092-841A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476019 | ||||||
chr2:171476125
|
A | T | 1 | a0001c0002t0002g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1092-735A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476125 | ||||||
chr2:171476149
|
CT | C | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1092-700delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 171476149 | |||||
chr2:171476335
|
A | G | 75 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1092-525A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476335 | ||||||
chr2:171476680
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1092-180C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476680 | ||||||
chr2:171476719
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1092-141T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476719 | ||||||
chr2:171476785
|
C | T | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1092-75C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476785 | ||||||
chr2:171477007
|
A | G | 5 | a0001c0001t0007g0017a0001c0001t0007g0195a0001c0001t0007g0197others(2): Show | 7 | HG01074.hp2 HG01261.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+57A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477007 | ||||||
chr2:171477142
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C | A | 89 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(86): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1182+192C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477142 | ||||||
chr2:171477185
|
CCTTTT | C | 9 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182+236_1182+240d others(7): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477185 | ||||||
chr2:171477453
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A | AT | 94 | a0001c0001t0001g0045a0001c0001t0001g0237a0001c0001t0001g0245others(91): Show | 119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1182+513dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 171477453 | |||||
chr2:171477503
|
G | T | 1 | a0001c0001t0001g0018 | 3 | HG01123.hp2 HG01516.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1183-484G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477503 | ||||||
chr2:171477704
|
A | ATCACTTG others(3): Show |
2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1183-282_1183-273d others(12): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 171477704 | |||||
chr2:171477756
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0154others(1): Show | 4 | HG02040.hp2 NA18989.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-231C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477756 | ||||||
chr2:171477879
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1183-108G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477879 | ||||||
chr2:171478084
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C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0172 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1266+14C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478084 | ||||||
chr2:171478121
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T | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0203others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+51T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478121 | ||||||
chr2:171478277
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G | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+207G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478277 | ||||||
chr2:171478435
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C | T | 75 | a0001c0001t0001g0153a0001c0002t0002g0003a0001c0002t0002g0007others(72): Show | 94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1266+365C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478435 | ||||||
chr2:171478506
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A | G | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1266+436A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478506 | ||||||
chr2:171478711
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A | G | 1 | a0001c0001t0006g0243 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1266+641A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478711 | ||||||
chr2:171478758
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A | T | 1 | a0001c0001t0001g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1266+688A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478758 | ||||||
chr2:171478879
|
CTG | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0141 | 3 | NA18969.hp1 NA18979.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1266+811_1266+812d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 171478879 | |||||
chr2:171479162
|
T | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0120others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1267-876T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171479162 | ||||||
chr2:171479256
|
G | A | 7 | a0001c0002t0002g0010a0001c0002t0002g0033a0001c0002t0002g0090others(4): Show | 10 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1267-782G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171479256 | ||||||
chr2:171479534
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AT | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1267-495delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 171479534 | |||||
chr2:171479769
|
G | A | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1267-269G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171479769 | ||||||
chr2:171480031
|
C | T | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
splice_region_variant&intron_variant | LOW | c.1267-7C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171480031 | ||||||
chr2:171480291
|
C | T | 5 | a0001c0005t0008g0055a0001c0005t0008g0056a0001c0005t0008g0059others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1422+98C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480291 | ||||||
chr2:171480473
|
G | A | 88 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(85): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1422+280G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480473 | ||||||
chr2:171480499
|
A | G | 74 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0008others(71): Show | 93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1422+306A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480499 | ||||||
chr2:171480753
|
C | T | 15 | a0002c0003t0003g0022a0002c0003t0003g0041a0002c0003t0003g0042others(12): Show | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1423-221C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480753 | ||||||
chr2:171480858
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A | G | 1 | a0001c0002t0002g0108 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1423-116A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480858 | ||||||
chr2:171480951
|
C | G | 9 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0243others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1423-23C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480951 |