geneid | 83852 |
---|---|
ensemblid | ENSG00000136169.17 |
hgncid | 20263 |
symbol | SETDB2 |
name | SET domain bifurcated histone lysine methyltransferase 2 |
refseq_nuc | NM_001160308.3 |
refseq_prot | NP_001153780.1 |
ensembl_nuc | ENST00000611815.2 |
ensembl_prot | ENSP00000482240.2 |
mane_status | MANE Select |
chr | chr13 |
start | 49444274 |
end | 49495003 |
strand | + |
ver | v1.2 |
region | chr13:49444274-49495003 |
region5000 | chr13:49439274-49500003 |
regionname0 | SETDB2_chr13_49444274_49495003 |
regionname5000 | SETDB2_chr13_49439274_49500003 |
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 | 0/1 | 707 | 289 | 54 | 48 | 161 | 8 | 17 | 127 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002 | 1/0 | 707 | 59 | 4 | 19 | 22 | 4 | 9 | 17 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003 | 0/0 | 707 | 34 | 16 | 3 | 9 | 0 | 6 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0004 | 0/0 | 707 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0005 | 0/0 | 707 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0006 | 0/0 | 707 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0007 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0008 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0009 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
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 | 0/1 | 2124 | 169 | 35 | 29 | 87 | 7 | 10 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0002 | 0/0 | 2124 | 115 | 17 | 19 | 72 | 1 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0003 | 1/0 | 2124 | 59 | 4 | 19 | 22 | 4 | 9 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0004 | 0/0 | 2124 | 34 | 16 | 3 | 9 | 0 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0005 | 0/0 | 2124 | 14 | 13 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0006 | 0/0 | 2124 | 5 | 0 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0007 | 0/0 | 2124 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0008 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0009 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0010 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0011 | 0/0 | 2111 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0012 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0013 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
c0014 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
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 | 0/1 | 4073 | 129 | 8 | 25 | 77 | 7 | 11 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0002 | 0/0 | 4075 | 44 | 1 | 13 | 29 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0003 | 0/0 | 4076 | 44 | 3 | 15 | 17 | 1 | 8 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0004 | 0/0 | 4074 | 37 | 4 | 1 | 27 | 1 | 4 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0005 | 0/0 | 4076 | 32 | 15 | 2 | 9 | 0 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0006 | 0/0 | 4074 | 14 | 13 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0007 | 0/0 | 4075 | 12 | 1 | 8 | 0 | 3 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0008 | 0/0 | 4074 | 10 | 0 | 0 | 10 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0009 | 0/0 | 4074 | 10 | 9 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0010 | 0/0 | 4074 | 6 | 5 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0011 | 0/0 | 4075 | 5 | 0 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0012 | 0/0 | 4077 | 5 | 5 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0013 | 0/0 | 4075 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0014 | 0/0 | 4074 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0015 | 0/0 | 4073 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0016 | 0/0 | 4075 | 4 | 3 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0017 | 0/0 | 4074 | 3 | 0 | 2 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0018 | 0/0 | 4076 | 3 | 2 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0019 | 0/0 | 4074 | 3 | 2 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0020 | 0/0 | 4074 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0021 | 0/0 | 4076 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0022 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0023 | 0/0 | 4073 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0024 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0025 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0026 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0027 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0028 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0029 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0030 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0031 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0032 | 0/0 | 4076 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0033 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0034 | 1/0 | 4080 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0035 | 0/0 | 4076 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0036 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0037 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0038 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0039 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0040 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0041 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0042 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0043 | 0/0 | 4073 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0044 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0045 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
t0046 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
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 | 0/1 | 2124 | 169 | 35 | 29 | 87 | 7 | 10 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002 | 0/0 | 2124 | 115 | 17 | 19 | 72 | 1 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0008 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0010 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0012 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0014 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003 | 1/0 | 2124 | 59 | 4 | 19 | 22 | 4 | 9 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003c0004 | 0/0 | 2124 | 34 | 16 | 3 | 9 | 0 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0004c0005 | 0/0 | 2124 | 14 | 13 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0005c0006 | 0/0 | 2124 | 5 | 0 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0006c0007 | 0/0 | 2124 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0007c0009 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0008c0013 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0009c0011 | 0/0 | 2111 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6196 | 128 | 8 | 25 | 77 | 7 | 10 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0005 | 0/0 | 6199 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0009 | 0/0 | 6197 | 10 | 9 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0010 | 0/0 | 6197 | 6 | 5 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0015 | 0/0 | 6196 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0016 | 0/0 | 6198 | 4 | 3 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0017 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0019 | 0/0 | 6197 | 3 | 2 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0023 | 0/0 | 6196 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0024 | 0/0 | 6198 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0037 | 0/0 | 6198 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0040 | 0/0 | 6196 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0041 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0042 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0044 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0045 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0001t0046 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0002 | 0/0 | 6198 | 38 | 1 | 8 | 28 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0004 | 0/0 | 6197 | 36 | 4 | 1 | 26 | 1 | 4 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0007 | 0/0 | 6198 | 6 | 1 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0008 | 0/0 | 6197 | 10 | 0 | 0 | 10 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0011 | 0/0 | 6198 | 3 | 0 | 3 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0012 | 0/0 | 6200 | 5 | 5 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0013 | 0/0 | 6198 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0017 | 0/0 | 6197 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0020 | 0/0 | 6197 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0022 | 0/0 | 6197 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0025 | 0/0 | 6197 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0026 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0027 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0028 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0029 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0002t0036 | 0/0 | 6198 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0008t0005 | 0/0 | 6199 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0010t0001 | 0/0 | 6196 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0012t0038 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0001c0014t0002 | 0/0 | 6198 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0003 | 0/0 | 6199 | 44 | 3 | 15 | 17 | 1 | 8 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0007 | 0/0 | 6198 | 6 | 0 | 3 | 0 | 3 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0014 | 0/0 | 6197 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0032 | 0/0 | 6199 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0033 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0034 | 1/0 | 6203 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0035 | 0/0 | 6199 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0002c0003t0043 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003c0004t0005 | 0/0 | 6199 | 28 | 11 | 2 | 9 | 0 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003c0004t0018 | 0/0 | 6199 | 3 | 2 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003c0004t0021 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003c0004t0030 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0003c0004t0031 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0004c0005t0006 | 0/0 | 6197 | 14 | 13 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0005c0006t0002 | 0/0 | 6198 | 5 | 0 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0006c0007t0011 | 0/0 | 6198 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0007c0009t0021 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0008c0013t0004 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
a0009c0011t0039 | 0/0 | 6194 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | copy fasta | chr13 | 49439274 | 49500003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0010g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0015g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0015g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0015g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0016g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0016g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0016g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0017g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0019g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0023g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0023g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0024g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0037g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0040g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0041g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0042g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0044g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0045g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0001t0046g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0004g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0007g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0007g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0008g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0011g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0011g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0011g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0012g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0013g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0013g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0013g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0013g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0017g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0020g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0020g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0020g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0022g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0022g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0025g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0026g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0027g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0028g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0029g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0002t0036g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0008t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0010t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0012t0038g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0001c0014t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0007g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0007g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0007g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0014g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0014g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0014g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0032g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0033g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0034g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0035g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0002c0003t0043g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0005g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0018g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0021g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0030g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0003c0004t0031g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0004c0005t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0005c0006t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0005c0006t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0005c0006t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0006c0007t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0006c0007t0011g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0007c0009t0021g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0008c0013t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
a0009c0011t0039g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00140 | hp2 | a0002 | c0003 | t0003 | g0285 | EUR | GBR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00280 | hp1 | a0002 | c0003 | t0007 | g0288 | EUR | FIN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00408 | hp2 | a0001 | c0002 | t0004 | g0376 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00438 | hp1 | a0001 | c0001 | t0041 | g0143 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00558 | hp2 | a0001 | c0002 | t0008 | g0377 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00597 | hp1 | a0001 | c0014 | t0002 | g0264 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00609 | hp2 | a0002 | c0003 | t0014 | g0321 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00639 | hp1 | a0001 | c0002 | t0007 | g0269 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0373 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00642 | hp2 | a0005 | c0006 | t0002 | g0013 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00733 | hp2 | a0002 | c0003 | t0003 | g0291 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00735 | hp1 | a0002 | c0003 | t0003 | g0317 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00738 | hp1 | a0006 | c0007 | t0011 | g0244 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00738 | hp2 | a0002 | c0003 | t0003 | g0302 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00741 | hp1 | a0001 | c0002 | t0007 | g0273 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01069 | hp1 | a0002 | c0003 | t0007 | g0017 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01070 | hp1 | a0002 | c0003 | t0003 | g0315 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01071 | hp2 | a0002 | c0003 | t0003 | g0018 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01074 | hp1 | a0001 | c0001 | t0016 | g0059 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01074 | hp2 | a0001 | c0002 | t0011 | g0268 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01081 | hp1 | a0001 | c0002 | t0011 | g0272 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01081 | hp2 | a0005 | c0006 | t0002 | g0236 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01099 | hp2 | a0002 | c0003 | t0003 | g0301 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01106 | hp1 | a0001 | c0001 | t0009 | g0062 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01106 | hp2 | a0002 | c0003 | t0003 | g0320 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01109 | hp1 | a0003 | c0004 | t0018 | g0196 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01109 | hp2 | a0003 | c0004 | t0005 | g0201 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01168 | hp2 | a0006 | c0007 | t0011 | g0245 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01243 | hp1 | a0004 | c0005 | t0006 | g0066 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0028 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01255 | hp2 | a0005 | c0006 | t0002 | g0014 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01257 | hp1 | a0001 | c0002 | t0017 | g0011 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01257 | hp2 | a0003 | c0004 | t0005 | g0202 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01258 | hp1 | a0001 | c0002 | t0011 | g0270 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01258 | hp2 | a0001 | c0002 | t0017 | g0011 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01261 | hp1 | a0002 | c0003 | t0007 | g0289 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01261 | hp2 | a0001 | c0002 | t0007 | g0271 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01358 | hp2 | a0001 | c0002 | t0007 | g0276 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0235 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01517 | hp2 | a0002 | c0003 | t0007 | g0017 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01884 | hp1 | a0004 | c0005 | t0006 | g0067 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01884 | hp2 | a0001 | c0001 | t0016 | g0189 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01928 | hp2 | a0002 | c0003 | t0003 | g0304 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01934 | hp1 | a0002 | c0003 | t0003 | g0303 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01943 | hp2 | a0002 | c0003 | t0003 | g0296 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01952 | hp2 | a0002 | c0003 | t0003 | g0298 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01975 | hp1 | a0002 | c0003 | t0032 | g0021 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01975 | hp2 | a0001 | c0001 | t0010 | g0158 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01978 | hp1 | a0002 | c0003 | t0003 | g0295 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01993 | hp1 | a0002 | c0003 | t0003 | g0297 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01993 | hp2 | a0001 | c0002 | t0007 | g0274 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0277 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02015 | hp1 | a0003 | c0004 | t0005 | g0231 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0379 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02027 | hp1 | a0001 | c0002 | t0004 | g0334 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02040 | hp2 | a0002 | c0003 | t0003 | g0332 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02056 | hp1 | a0002 | c0003 | t0003 | g0327 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02056 | hp2 | a0001 | c0002 | t0004 | g0359 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02071 | hp2 | a0001 | c0002 | t0013 | g0262 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02080 | hp1 | a0001 | c0002 | t0013 | g0263 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02083 | hp1 | a0002 | c0003 | t0043 | g0306 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02083 | hp2 | a0003 | c0004 | t0005 | g0214 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02132 | hp1 | a0001 | c0002 | t0026 | g0020 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02132 | hp2 | a0003 | c0004 | t0005 | g0205 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02135 | hp1 | a0001 | c0002 | t0004 | g0357 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02145 | hp1 | a0004 | c0005 | t0006 | g0065 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02145 | hp2 | a0003 | c0004 | t0005 | g0223 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02148 | hp1 | a0002 | c0003 | t0003 | g0300 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02155 | hp1 | a0001 | c0002 | t0004 | g0348 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02165 | hp1 | a0002 | c0003 | t0014 | g0324 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02257 | hp1 | a0001 | c0001 | t0044 | g0188 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02257 | hp2 | a0004 | c0005 | t0006 | g0074 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02258 | hp1 | a0004 | c0005 | t0006 | g0064 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02258 | hp2 | a0001 | c0001 | t0046 | g0159 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0278 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02273 | hp2 | a0002 | c0003 | t0003 | g0299 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02280 | hp1 | a0002 | c0003 | t0033 | g0309 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0170 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02293 | hp1 | a0005 | c0006 | t0002 | g0013 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02300 | hp1 | a0005 | c0006 | t0002 | g0014 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02451 | hp1 | a0004 | c0005 | t0006 | g0070 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02451 | hp2 | a0003 | c0004 | t0005 | g0209 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02572 | hp1 | a0003 | c0004 | t0005 | g0210 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02572 | hp2 | a0001 | c0002 | t0020 | g0275 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02602 | hp1 | a0001 | c0002 | t0025 | g0375 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02602 | hp2 | a0003 | c0004 | t0005 | g0200 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02622 | hp1 | a0003 | c0004 | t0005 | g0204 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02622 | hp2 | a0004 | c0005 | t0006 | g0075 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0169 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02647 | hp1 | a0003 | c0004 | t0021 | g0193 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02647 | hp2 | a0001 | c0001 | t0010 | g0052 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02698 | hp1 | a0001 | c0002 | t0004 | g0365 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02698 | hp2 | a0003 | c0004 | t0005 | g0213 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02717 | hp1 | a0001 | c0008 | t0005 | g0008 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0192 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02723 | hp2 | a0001 | c0001 | t0016 | g0061 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02738 | hp2 | a0002 | c0003 | t0003 | g0307 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02818 | hp1 | a0001 | c0002 | t0012 | g0281 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02818 | hp2 | a0004 | c0005 | t0006 | g0068 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02886 | hp1 | a0003 | c0004 | t0005 | g0206 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02886 | hp2 | a0001 | c0002 | t0027 | g0333 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02895 | hp2 | a0003 | c0004 | t0018 | g0195 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02896 | hp1 | a0001 | c0002 | t0020 | g0267 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02896 | hp2 | a0004 | c0005 | t0006 | g0073 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02897 | hp2 | a0004 | c0005 | t0006 | g0063 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02922 | hp1 | a0001 | c0001 | t0019 | g0027 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02922 | hp2 | a0001 | c0002 | t0012 | g0280 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02970 | hp1 | a0003 | c0004 | t0030 | g0198 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02976 | hp1 | a0007 | c0009 | t0021 | g0194 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02976 | hp2 | a0003 | c0004 | t0005 | g0208 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03017 | hp1 | a0001 | c0002 | t0004 | g0374 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03017 | hp2 | a0002 | c0003 | t0035 | g0293 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03041 | hp1 | a0001 | c0001 | t0024 | g0057 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03041 | hp2 | a0003 | c0004 | t0005 | g0207 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03098 | hp1 | a0004 | c0005 | t0006 | g0071 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0076 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03130 | hp2 | a0001 | c0002 | t0004 | g0265 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0077 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03139 | hp2 | a0001 | c0008 | t0005 | g0008 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0079 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0337 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03209 | hp2 | a0002 | c0003 | t0003 | g0082 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03225 | hp2 | a0001 | c0001 | t0024 | g0060 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03239 | hp1 | a0002 | c0003 | t0003 | g0292 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03453 | hp1 | a0001 | c0001 | t0019 | g0026 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03453 | hp2 | a0001 | c0002 | t0012 | g0016 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0058 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03490 | hp1 | a0003 | c0004 | t0005 | g0010 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03492 | hp1 | a0003 | c0004 | t0005 | g0010 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03492 | hp2 | a0002 | c0003 | t0003 | g0312 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03516 | hp1 | a0003 | c0004 | t0005 | g0211 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03540 | hp2 | a0001 | c0001 | t0040 | g0115 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03579 | hp1 | a0001 | c0002 | t0028 | g0228 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03579 | hp2 | a0002 | c0003 | t0003 | g0083 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03688 | hp2 | a0001 | c0002 | t0004 | g0360 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03704 | hp2 | a0001 | c0010 | t0001 | g0106 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03710 | hp2 | a0002 | c0003 | t0003 | g0313 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03834 | hp1 | a0002 | c0003 | t0003 | g0328 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03927 | hp2 | a0002 | c0003 | t0003 | g0314 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03942 | hp1 | a0002 | c0003 | t0003 | g0305 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03942 | hp2 | a0003 | c0004 | t0005 | g0212 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG04199 | hp2 | a0003 | c0004 | t0005 | g0199 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG04204 | hp1 | a0001 | c0002 | t0004 | g0361 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18522 | hp1 | a0001 | c0002 | t0012 | g0282 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0266 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18612 | hp2 | a0001 | c0001 | t0042 | g0137 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18747 | hp2 | a0001 | c0002 | t0013 | g0242 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18939 | hp2 | a0001 | c0002 | t0004 | g0220 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18940 | hp1 | a0001 | c0002 | t0004 | g0363 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18940 | hp2 | a0009 | c0011 | t0039 | g0048 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18942 | hp1 | a0001 | c0002 | t0004 | g0355 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18943 | hp1 | a0001 | c0002 | t0004 | g0354 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18943 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18945 | hp2 | a0001 | c0002 | t0004 | g0341 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18947 | hp1 | a0003 | c0004 | t0005 | g0216 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18947 | hp2 | a0002 | c0003 | t0003 | g0283 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18948 | hp1 | a0001 | c0002 | t0004 | g0342 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18950 | hp1 | a0002 | c0003 | t0003 | g0311 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18952 | hp1 | a0001 | c0002 | t0022 | g0343 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18953 | hp1 | a0003 | c0004 | t0005 | g0378 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18954 | hp1 | a0001 | c0001 | t0017 | g0163 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18959 | hp2 | a0001 | c0002 | t0004 | g0338 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18960 | hp1 | a0003 | c0004 | t0005 | g0215 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18961 | hp2 | a0002 | c0003 | t0003 | g0329 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18962 | hp2 | a0003 | c0004 | t0005 | g0217 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18964 | hp2 | a0002 | c0003 | t0014 | g0325 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18966 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18969 | hp1 | a0001 | c0002 | t0013 | g0249 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18969 | hp2 | a0001 | c0001 | t0023 | g0119 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18973 | hp2 | a0001 | c0002 | t0008 | g0370 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18974 | hp1 | a0001 | c0002 | t0022 | g0340 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18977 | hp1 | a0001 | c0002 | t0004 | g0353 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18980 | hp2 | a0002 | c0003 | t0014 | g0326 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18983 | hp1 | a0001 | c0002 | t0008 | g0371 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18984 | hp2 | a0002 | c0003 | t0003 | g0323 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18985 | hp2 | a0001 | c0002 | t0004 | g0350 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18986 | hp1 | a0002 | c0003 | t0003 | g0322 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18988 | hp1 | a0001 | c0002 | t0008 | g0367 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18989 | hp2 | a0001 | c0002 | t0004 | g0358 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18994 | hp2 | a0002 | c0003 | t0003 | g0331 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18998 | hp1 | a0001 | c0002 | t0008 | g0020 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19001 | hp2 | a0003 | c0004 | t0005 | g0219 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19003 | hp2 | a0001 | c0002 | t0008 | g0366 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19004 | hp1 | a0002 | c0003 | t0003 | g0284 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19004 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19005 | hp1 | a0001 | c0012 | t0038 | g0142 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19006 | hp1 | a0002 | c0003 | t0003 | g0318 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19007 | hp1 | a0001 | c0002 | t0008 | g0368 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19009 | hp1 | a0001 | c0001 | t0023 | g0132 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0349 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19010 | hp2 | a0002 | c0003 | t0003 | g0316 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19011 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19030 | hp1 | a0001 | c0001 | t0045 | g0190 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19030 | hp2 | a0003 | c0004 | t0005 | g0203 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19055 | hp2 | a0002 | c0003 | t0003 | g0330 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19057 | hp1 | a0001 | c0001 | t0015 | g0037 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19057 | hp2 | a0001 | c0002 | t0004 | g0364 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19060 | hp1 | a0001 | c0002 | t0004 | g0344 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19062 | hp1 | a0001 | c0002 | t0004 | g0346 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19064 | hp2 | a0001 | c0002 | t0008 | g0019 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19066 | hp2 | a0001 | c0002 | t0004 | g0339 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19068 | hp1 | a0001 | c0002 | t0004 | g0351 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19072 | hp1 | a0001 | c0002 | t0036 | g0234 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19072 | hp2 | a0001 | c0002 | t0004 | g0352 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19076 | hp1 | a0001 | c0002 | t0004 | g0345 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19078 | hp1 | a0001 | c0002 | t0004 | g0347 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19078 | hp2 | a0001 | c0001 | t0037 | g0100 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19081 | hp2 | a0001 | c0002 | t0004 | g0362 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19085 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19086 | hp2 | a0002 | c0003 | t0003 | g0319 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19087 | hp2 | a0003 | c0004 | t0005 | g0218 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19088 | hp2 | a0001 | c0002 | t0008 | g0019 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19089 | hp1 | a0001 | c0001 | t0015 | g0036 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19089 | hp2 | a0002 | c0003 | t0003 | g0310 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19090 | hp2 | a0001 | c0002 | t0008 | g0369 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19240 | hp1 | a0003 | c0004 | t0005 | g0224 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA19240 | hp2 | a0004 | c0005 | t0006 | g0072 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | ASW | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20129 | hp2 | a0003 | c0004 | t0018 | g0197 | AFR | ASW | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0335 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20805 | hp2 | a0002 | c0003 | t0007 | g0287 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20905 | hp1 | a0002 | c0003 | t0003 | g0294 | SAS | GIH | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0229 | SAS | GIH | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01123 | hp1 | a0002 | c0003 | t0007 | g0290 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02109 | hp1 | a0004 | c0005 | t0006 | g0022 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02109 | hp2 | a0003 | c0004 | t0031 | g0221 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02559 | hp1 | a0001 | c0002 | t0007 | g0243 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0081 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03471 | hp1 | a0001 | c0002 | t0012 | g0016 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG03471 | hp2 | a0001 | c0002 | t0020 | g0227 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
HG06807 | hp2 | a0002 | c0003 | t0003 | g0018 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA18955 | hp2 | a0008 | c0013 | t0004 | g0356 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA20300 | hp2 | a0004 | c0005 | t0006 | g0069 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA21309 | hp1 | a0001 | c0002 | t0029 | g0372 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
NA21309 | hp2 | a0003 | c0004 | t0005 | g0222 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0034 | g0308 | REF | REF | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49476484
|
A | G | 6 | a0001a0004a0005others(3): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
missense_variant | MODERATE | c.314A>G | p.Glu105Gly | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/14 | 1239/6203 | 314/2124 | 105/707 | chr13 | 49476484 | ||
chr13:49476973
|
A | G | 1 | a0008 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.803A>G | p.Tyr268Cys | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/14 | 1728/6203 | 803/2124 | 268/707 | chr13 | 49476973 | ||
chr13:49482767
|
A | T | 1 | a0004 | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.1187A>T | p.Lys396Ile | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2112/6203 | 1187/2124 | 396/707 | chr13 | 49482767 | ||
chr13:49482790
|
G | A | 1 | a0005 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.1210G>A | p.Gly404Arg | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2135/6203 | 1210/2124 | 404/707 | chr13 | 49482790 | ||
chr13:49482860
|
G | C | 1 | a0007 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1280G>C | p.Cys427Ser | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2205/6203 | 1280/2124 | 427/707 | chr13 | 49482860 | ||
chr13:49482907
|
G | A | 1 | a0006 | 2 | HG00738.hp1 HG01168.hp2 |
missense_variant | MODERATE | c.1327G>A | p.Ala443Thr | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2252/6203 | 1327/2124 | 443/707 | chr13 | 49482907 | ||
chr13:49482961
|
G | A | 8 | a0001a0003a0004others(5): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
missense_variant&splice_region_variant | MODERATE | c.1381G>A | p.Val461Met | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2306/6203 | 1381/2124 | 461/707 | chr13 | 49482961 | ||
chr13:49490897
|
TTCTTCAC others(13): Show |
T | 1 | a0009 | 1 | NA18940.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1994_2006+7delTCTT others(16): Show |
p.Phe665fs | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/14 | 2919/6203 | 1994/2124 | 665/707 | chr13 | 49490897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49467916
|
C | T | 1 | a0001c0008 | 2 | HG02717.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.261C>T | p.Pro87Pro | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/14 | 1186/6203 | 261/2124 | 87/707 | chr13 | 49467916 | ||
chr13:49476650
|
C | T | 1 | a0001c0014 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.480C>T | p.His160His | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/14 | 1405/6203 | 480/2124 | 160/707 | chr13 | 49476650 | ||
chr13:49482768
|
A | G | 1 | a0001c0012 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1188A>G | p.Lys396Lys | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2113/6203 | 1188/2124 | 396/707 | chr13 | 49482768 | ||
chr13:49482780
|
T | C | 1 | a0001c0010 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1200T>C | p.Ile400Ile | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2125/6203 | 1200/2124 | 400/707 | chr13 | 49482780 | ||
chr13:49483497
|
A | G | 5 | a0001c0001a0001c0008a0001c0010others(2): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
synonymous_variant | LOW | c.1416A>G | p.Gln472Gln | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/14 | 2341/6203 | 1416/2124 | 472/707 | chr13 | 49483497 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49444373
|
AC | A | 1 | a0001c0002t0020 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-824delC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7519 | INFO_REALIGN_3_PRIME | chr13 | 49444373 | ||||
chr13:49444482
|
G | A | 1 | a0001c0002t0025 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-717G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7412 | chr13 | 49444482 | |||||
chr13:49444505
|
C | T | 1 | a0001c0002t0012 | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-694C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7389 | chr13 | 49444505 | |||||
chr13:49444554
|
G | C | 2 | a0003c0004t0021a0007c0009t0021 | 2 | HG02647.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-645G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7340 | chr13 | 49444554 | |||||
chr13:49444602
|
G | C | 1 | a0001c0002t0012 | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-597G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7292 | chr13 | 49444602 | |||||
chr13:49444641
|
C | T | 2 | a0001c0001t0010a0001c0001t0046 | 7 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-558C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7253 | chr13 | 49444641 | |||||
chr13:49444686
|
C | T | 2 | a0001c0002t0011a0006c0007t0011 | 5 | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-513C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7208 | chr13 | 49444686 | |||||
chr13:49444692
|
G | A | 1 | a0001c0002t0026 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-507G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7202 | chr13 | 49444692 | |||||
chr13:49444704
|
CA | C | 11 | a0001c0001t0001a0001c0001t0015a0001c0001t0023others(8): Show | 142 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-494delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7189 | chr13 | 49444704 | |||||
chr13:49444705
|
A | G | 8 | a0001c0001t0009a0001c0001t0010a0001c0001t0016others(5): Show | 28 | HG01074.hp1 HG01106.hp1 HG01243.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-494A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7189 | chr13 | 49444705 | |||||
chr13:49444706
|
T | G | 11 | a0001c0001t0001a0001c0001t0015a0001c0001t0023others(8): Show | 142 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-493T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7188 | chr13 | 49444706 | |||||
chr13:49444740
|
G | A | 1 | a0001c0002t0012 | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-459G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7154 | chr13 | 49444740 | |||||
chr13:49451874
|
T | G | 1 | a0001c0002t0027 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/14 | 20 | chr13 | 49451874 | |||||
chr13:49491917
|
T | A | 1 | a0001c0001t0015 | 4 | NA19004.hp2 NA19011.hp2 NA19057.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*68T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 68 | chr13 | 49491917 | |||||
chr13:49492222
|
C | A | 1 | a0001c0001t0044 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 373 | chr13 | 49492222 | |||||
chr13:49492252
|
A | G | 1 | a0004c0005t0006 | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*403A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 403 | chr13 | 49492252 | |||||
chr13:49492353
|
A | G | 1 | a0001c0001t0023 | 2 | NA18969.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*504A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 504 | chr13 | 49492353 | |||||
chr13:49492388
|
G | A | 20 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(17): Show | 172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 539 | chr13 | 49492388 | |||||
chr13:49492495
|
C | T | 1 | a0001c0002t0036 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 646 | chr13 | 49492495 | |||||
chr13:49492507
|
T | A | 49 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(46): Show | 353 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*658T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 658 | chr13 | 49492507 | |||||
chr13:49492527
|
G | A | 1 | a0001c0002t0008 | 10 | HG00558.hp2 NA18973.hp2 NA18983.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*678G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 678 | chr13 | 49492527 | |||||
chr13:49492585
|
C | T | 49 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(46): Show | 353 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 736 | chr13 | 49492585 | |||||
chr13:49492842
|
T | C | 40 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(37): Show | 309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*993T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 993 | chr13 | 49492842 | |||||
chr13:49492948
|
ACT | A | 2 | a0002c0003t0014a0002c0003t0043 | 5 | HG00609.hp2 HG02083.hp1 HG02165.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1107_*1108delTC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1107 | INFO_REALIGN_3_PRIME | chr13 | 49492948 | ||||
chr13:49492962
|
A | G | 5 | a0001c0002t0002a0001c0002t0013a0001c0002t0036others(2): Show | 49 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1113A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1113 | chr13 | 49492962 | |||||
chr13:49492968
|
GCA | G | 39 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(36): Show | 308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*1135_*1136delAC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1135 | INFO_REALIGN_3_PRIME | chr13 | 49492968 | ||||
chr13:49493049
|
A | C | 5 | a0001c0001t0005a0001c0002t0012a0001c0008t0005others(2): Show | 38 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1200A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1200 | chr13 | 49493049 | |||||
chr13:49493052
|
C | CT | 13 | a0001c0001t0016a0001c0001t0024a0001c0002t0002others(10): Show | 80 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1213dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 49493052 | ||||
chr13:49493110
|
G | C | 40 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(37): Show | 309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*1261G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1261 | chr13 | 49493110 | |||||
chr13:49493121
|
T | C | 1 | a0001c0002t0013 | 4 | HG02071.hp2 HG02080.hp1 NA18747.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1272T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1272 | chr13 | 49493121 | |||||
chr13:49493152
|
C | T | 1 | a0001c0001t0041 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1303C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1303 | chr13 | 49493152 | |||||
chr13:49493250
|
G | A | 1 | a0004c0005t0006 | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1401G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1401 | chr13 | 49493250 | |||||
chr13:49493306
|
T | C | 40 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(37): Show | 309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*1457T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1457 | chr13 | 49493306 | |||||
chr13:49493307
|
G | A | 20 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(17): Show | 173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1458G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1458 | chr13 | 49493307 | |||||
chr13:49493329
|
G | A | 1 | a0001c0012t0038 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1480G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1480 | chr13 | 49493329 | |||||
chr13:49493357
|
T | C | 1 | a0002c0003t0032 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1508 | chr13 | 49493357 | |||||
chr13:49493636
|
T | C | 1 | a0002c0003t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1787T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1787 | chr13 | 49493636 | |||||
chr13:49493737
|
G | C | 3 | a0003c0004t0018a0003c0004t0021a0007c0009t0021 | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1888G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1888 | chr13 | 49493737 | |||||
chr13:49493788
|
T | C | 3 | a0003c0004t0018a0003c0004t0021a0007c0009t0021 | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1939T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1939 | chr13 | 49493788 | |||||
chr13:49493829
|
C | A | 1 | a0001c0001t0046 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1980 | chr13 | 49493829 | |||||
chr13:49493848
|
T | C | 1 | a0003c0004t0030 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1999 | chr13 | 49493848 | |||||
chr13:49494168
|
C | T | 2 | a0001c0001t0044a0001c0001t0045 | 2 | HG02257.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2319C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2319 | chr13 | 49494168 | |||||
chr13:49494169
|
A | G | 1 | a0001c0001t0040 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2320A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2320 | chr13 | 49494169 | |||||
chr13:49494211
|
G | A | 1 | a0001c0001t0024 | 2 | HG03041.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2362G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2362 | chr13 | 49494211 | |||||
chr13:49494228
|
A | G | 1 | a0002c0003t0035 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2379A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2379 | chr13 | 49494228 | |||||
chr13:49494241
|
T | G | 1 | a0001c0001t0040 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2392T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2392 | chr13 | 49494241 | |||||
chr13:49494251
|
G | A | 20 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(17): Show | 172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*2402G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2402 | chr13 | 49494251 | |||||
chr13:49494434
|
G | A | 1 | a0001c0001t0019 | 3 | HG01243.hp2 HG02922.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2585G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2585 | chr13 | 49494434 | |||||
chr13:49494488
|
T | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2639 | chr13 | 49494488 | |||||
chr13:49494489
|
A | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2640A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2640 | chr13 | 49494489 | |||||
chr13:49494490
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2641C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2641 | chr13 | 49494490 | |||||
chr13:49494491
|
T | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2642T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2642 | chr13 | 49494491 | |||||
chr13:49494492
|
A | G | 48 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(45): Show | 352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*2643A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2643 | chr13 | 49494492 | |||||
chr13:49494493
|
T | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2644T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2644 | chr13 | 49494493 | |||||
chr13:49494495
|
A | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2646A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2646 | chr13 | 49494495 | |||||
chr13:49494497
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2648 | chr13 | 49494497 | |||||
chr13:49494497
|
C | T | 1 | a0003c0004t0031 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2648 | chr13 | 49494497 | |||||
chr13:49494498
|
T | C | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2649T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2649 | chr13 | 49494498 | |||||
chr13:49494499
|
G | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2650 | chr13 | 49494499 | |||||
chr13:49494502
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2653A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2653 | chr13 | 49494502 | |||||
chr13:49494507
|
G | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2658 | chr13 | 49494507 | |||||
chr13:49494511
|
A | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2662 | chr13 | 49494511 | |||||
chr13:49494517
|
T | TTGGTTTA others(4): Show |
1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2668_*2669insTGGT others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2669 | chr13 | 49494517 | |||||
chr13:49494525
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2676T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2676 | chr13 | 49494525 | |||||
chr13:49494546
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2697A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2697 | chr13 | 49494546 | |||||
chr13:49494548
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2699C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2699 | chr13 | 49494548 | |||||
chr13:49494551
|
G | C | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2702G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2702 | chr13 | 49494551 | |||||
chr13:49494552
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2703C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2703 | chr13 | 49494552 | |||||
chr13:49494553
|
T | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2704T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2704 | chr13 | 49494553 | |||||
chr13:49494584
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2735 | chr13 | 49494584 | |||||
chr13:49494594
|
C | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2745C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2745 | chr13 | 49494594 | |||||
chr13:49494596
|
T | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2747T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2747 | chr13 | 49494596 | |||||
chr13:49494644
|
A | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2795A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2795 | chr13 | 49494644 | |||||
chr13:49494647
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2798A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2798 | chr13 | 49494647 | |||||
chr13:49494650
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2801A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2801 | chr13 | 49494650 | |||||
chr13:49494670
|
GGTCT | G | 55 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(52): Show | 405 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(402): Show |
3_prime_UTR_variant | MODIFIER | c.*2827_*2830delTCTG | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2827 | INFO_REALIGN_3_PRIME | chr13 | 49494670 | ||||
chr13:49494697
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2848C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2848 | chr13 | 49494697 | |||||
chr13:49494709
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2860 | chr13 | 49494709 | |||||
chr13:49494712
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2863T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2863 | chr13 | 49494712 | |||||
chr13:49494745
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2896C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2896 | chr13 | 49494745 | |||||
chr13:49494761
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2912A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2912 | chr13 | 49494761 | |||||
chr13:49494762
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2913T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2913 | chr13 | 49494762 | |||||
chr13:49494765
|
T | C | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2916T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2916 | chr13 | 49494765 | |||||
chr13:49494766
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2917C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2917 | chr13 | 49494766 | |||||
chr13:49494767
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2918T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2918 | chr13 | 49494767 | |||||
chr13:49494768
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2919C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2919 | chr13 | 49494768 | |||||
chr13:49494796
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2947T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2947 | chr13 | 49494796 | |||||
chr13:49494797
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2948C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2948 | chr13 | 49494797 | |||||
chr13:49494800
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2951C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2951 | chr13 | 49494800 | |||||
chr13:49494801
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2952T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2952 | chr13 | 49494801 | |||||
chr13:49494803
|
T | C | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2954T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2954 | chr13 | 49494803 | |||||
chr13:49494804
|
A | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2955A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2955 | chr13 | 49494804 | |||||
chr13:49494837
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2988C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2988 | chr13 | 49494837 | |||||
chr13:49494841
|
T | A | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2992T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2992 | chr13 | 49494841 | |||||
chr13:49494843
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2994A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2994 | chr13 | 49494843 | |||||
chr13:49494846
|
C | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2997C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2997 | chr13 | 49494846 | |||||
chr13:49494849
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3000C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3000 | chr13 | 49494849 | |||||
chr13:49494857
|
C | G | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3008C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3008 | chr13 | 49494857 | |||||
chr13:49494861
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3012A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3012 | chr13 | 49494861 | |||||
chr13:49494865
|
A | T | 1 | a0009c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3016A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3016 | chr13 | 49494865 | |||||
chr13:49494940
|
C | T | 1 | a0001c0002t0029 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3091C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3091 | chr13 | 49494940 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49444985
|
G | T | 1 | a0001c0002t0004g0379 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-342+128G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49444985 | ||||||
chr13:49445012
|
A | T | 1 | a0003c0004t0005g0378 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-342+155A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445012 | ||||||
chr13:49445128
|
G | C | 1 | a0002c0003t0032g0021 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-342+271G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445128 | ||||||
chr13:49445144
|
C | G | 49 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(46): Show | 50 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.-342+287C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445144 | ||||||
chr13:49445240
|
T | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(176): Show | 188 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.-342+383T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445240 | ||||||
chr13:49445471
|
C | T | 1 | a0001c0001t0010g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-342+614C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445471 | ||||||
chr13:49445681
|
C | A | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-342+824C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445681 | ||||||
chr13:49445936
|
C | CAA | 112 | a0001c0001t0001g0191a0001c0001t0005g0336a0001c0001t0005g0337others(109): Show | 122 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-342+1094_-342+109 others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49445936 | |||||
chr13:49445936
|
C | CAAA | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 182 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.-342+1093_-342+109 others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49445936 | |||||
chr13:49445936
|
C | CAAAA | 43 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-342+1092_-342+109 others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49445936 | |||||
chr13:49445972
|
G | T | 3 | a0001c0001t0016g0189a0001c0001t0044g0188a0001c0001t0045g0190 | 3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-342+1115G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445972 | ||||||
chr13:49445986
|
A | G | 1 | a0001c0002t0008g0377 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-342+1129A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445986 | ||||||
chr13:49446144
|
C | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(152): Show | 162 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-342+1287C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49446144 | ||||||
chr13:49446280
|
G | A | 2 | a0001c0002t0002g0229a0001c0002t0002g0230 | 2 | HG01192.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-342+1423G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49446280 | ||||||
chr13:49446783
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-342+1926C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49446783 | ||||||
chr13:49447123
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-342+2266A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447123 | ||||||
chr13:49447314
|
A | G | 4 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-342+2457A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447314 | ||||||
chr13:49447406
|
G | A | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.-342+2549G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447406 | ||||||
chr13:49447415
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-342+2558T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447415 | ||||||
chr13:49447470
|
G | A | 2 | a0002c0003t0003g0283a0002c0003t0003g0284 | 2 | NA18947.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-342+2613G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447470 | ||||||
chr13:49447513
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-342+2656G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447513 | ||||||
chr13:49447563
|
T | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG00140.hp2 HG01346.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-342+2706T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447563 | ||||||
chr13:49447918
|
G | A | 1 | a0001c0002t0002g0232 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-342+3061G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447918 | ||||||
chr13:49447953
|
G | C | 323 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(320): Show | 344 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.-342+3096G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447953 | ||||||
chr13:49447973
|
A | G | 7 | a0001c0002t0017g0011a0001c0002t0028g0228a0003c0004t0018g0195others(4): Show | 8 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-342+3116A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447973 | ||||||
chr13:49448325
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00438.hp2 NA18960.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-341-3228A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448325 | ||||||
chr13:49448490
|
C | T | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-341-3063C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448490 | ||||||
chr13:49448628
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-341-2925G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448628 | ||||||
chr13:49448707
|
C | T | 7 | a0001c0001t0001g0056a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG00609.hp1 HG01255.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-341-2846C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448707 | ||||||
chr13:49448737
|
C | T | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.-341-2816C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448737 | ||||||
chr13:49448746
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0171others(4): Show | 8 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-341-2807A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448746 | ||||||
chr13:49448810
|
C | T | 1 | a0002c0003t0003g0332 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-341-2743C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448810 | ||||||
chr13:49448846
|
A | G | 2 | a0001c0001t0010g0169a0001c0001t0010g0170 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-341-2707A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448846 | ||||||
chr13:49448921
|
G | A | 1 | a0001c0002t0027g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-341-2632G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448921 | ||||||
chr13:49449000
|
C | A | 5 | a0002c0003t0007g0017a0002c0003t0007g0287a0002c0003t0007g0288others(2): Show | 6 | HG00280.hp1 HG01069.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-341-2553C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449000 | ||||||
chr13:49449031
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-341-2522G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449031 | ||||||
chr13:49449346
|
G | T | 1 | a0001c0008t0005g0008 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-341-2207G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449346 | ||||||
chr13:49449438
|
A | G | 1 | a0001c0001t0045g0190 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-341-2115A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449438 | ||||||
chr13:49449943
|
G | A | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-341-1610G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449943 | ||||||
chr13:49449946
|
T | A | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-341-1607T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449946 | ||||||
chr13:49450088
|
C | T | 1 | a0001c0002t0004g0376 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-341-1465C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450088 | ||||||
chr13:49450718
|
C | G | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-341-835C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450718 | ||||||
chr13:49450735
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.-341-818A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450735 | ||||||
chr13:49450741
|
A | G | 46 | a0001c0002t0004g0334a0001c0002t0004g0335a0001c0002t0004g0338others(43): Show | 47 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.-341-812A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450741 | ||||||
chr13:49450851
|
A | G | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-341-702A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450851 | ||||||
chr13:49450866
|
T | G | 1 | a0001c0008t0005g0008 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-341-687T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450866 | ||||||
chr13:49450903
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-341-650A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450903 | ||||||
chr13:49450918
|
CTAAA | C | 3 | a0001c0002t0002g0277a0001c0002t0002g0278a0001c0002t0002g0279 | 3 | HG01981.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-341-632_-341-629d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450918 | |||||
chr13:49450941
|
ATAT | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-341-606_-341-604d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450941 | |||||
chr13:49450945
|
TATTA | T | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-341-601_-341-598d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450945 | |||||
chr13:49450966
|
AAATTT | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-341-582_-341-578d others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450966 | |||||
chr13:49450977
|
T | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG01255.hp1 HG01496.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-341-576T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450977 | ||||||
chr13:49451006
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-341-547C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451006 | ||||||
chr13:49451066
|
G | A | 2 | a0003c0004t0021g0193a0007c0009t0021g0194 | 2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-341-487G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451066 | ||||||
chr13:49451103
|
AAAATT | A | 7 | a0001c0002t0002g0012a0001c0002t0002g0233a0001c0002t0002g0235others(4): Show | 10 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-341-445_-341-441d others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451103 | |||||
chr13:49451195
|
G | A | 30 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(27): Show | 31 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-341-358G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451195 | ||||||
chr13:49451204
|
A | C | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-341-349A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451204 | ||||||
chr13:49451336
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01515.hp2 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-341-217T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451336 | ||||||
chr13:49451359
|
T | A | 322 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 343 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.-341-194T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451359 | ||||||
chr13:49451478
|
C | CAT | 31 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(28): Show | 32 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-341-48_-341-47dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
C | CATAT | 10 | a0001c0001t0001g0090a0001c0001t0024g0057a0001c0002t0004g0334others(7): Show | 10 | HG00733.hp2 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.-341-50_-341-47dup others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
CAT | C | 90 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0056others(87): Show | 96 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-341-48_-341-47del others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
CATAT | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(163): Show | 180 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-341-50_-341-47del others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
CATATAT | C | 22 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0001t0016g0189others(19): Show | 25 | HG00639.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-341-52_-341-47del others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0045g0190a0001c0002t0012g0282a0002c0003t0003g0082others(1): Show | 4 | HG03209.hp2 HG03579.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-341-54_-341-47del others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
CATATATA others(3): Show |
C | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-341-56_-341-47del others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451478
|
CATATATA others(5): Show |
C | 1 | a0001c0002t0007g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-341-58_-341-47del others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | |||||
chr13:49451485
|
A | G | 2 | a0001c0001t0005g0336a0001c0001t0005g0337 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-341-68A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451485 | ||||||
chr13:49452110
|
CT | C | 32 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(29): Show | 33 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.16+213delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49452110 | |||||
chr13:49452149
|
T | C | 1 | a0001c0002t0027g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+240T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452149 | ||||||
chr13:49452200
|
C | T | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+291C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452200 | ||||||
chr13:49452525
|
G | A | 1 | a0001c0002t0027g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+616G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452525 | ||||||
chr13:49452590
|
A | G | 380 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(377): Show | 405 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.16+681A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452590 | ||||||
chr13:49452656
|
C | T | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+747C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452656 | ||||||
chr13:49452758
|
A | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0094others(19): Show | 23 | HG00438.hp1 HG00558.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.16+849A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452758 | ||||||
chr13:49452812
|
C | T | 2 | a0003c0004t0021g0193a0007c0009t0021g0194 | 2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.16+903C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452812 | ||||||
chr13:49452844
|
A | G | 1 | a0007c0009t0021g0194 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16+935A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452844 | ||||||
chr13:49452928
|
G | A | 1 | a0001c0001t0044g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.16+1019G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452928 | ||||||
chr13:49453059
|
A | G | 1 | a0002c0003t0003g0328 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.16+1150A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453059 | ||||||
chr13:49453134
|
C | A | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(325): Show | 349 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(346): Show |
intron_variant | MODIFIER | c.16+1225C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453134 | ||||||
chr13:49453197
|
T | C | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.16+1288T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453197 | ||||||
chr13:49453302
|
T | C | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+1393T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453302 | ||||||
chr13:49453303
|
C | CT | 30 | a0001c0001t0001g0051a0001c0002t0004g0220a0003c0004t0005g0010others(27): Show | 31 | HG00280.hp2 HG01109.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.16+1405dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49453303 | |||||
chr13:49453513
|
G | C | 1 | a0001c0002t0012g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.16+1604G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453513 | ||||||
chr13:49453566
|
G | C | 48 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+1657G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453566 | ||||||
chr13:49453627
|
C | T | 5 | a0001c0002t0004g0335a0001c0002t0004g0373a0001c0002t0004g0374others(2): Show | 5 | HG00642.hp1 HG02602.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+1718C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453627 | ||||||
chr13:49453710
|
C | T | 48 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+1801C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453710 | ||||||
chr13:49453870
|
G | GTA | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.16+1974_16+1975dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49453870 | |||||
chr13:49454174
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.16+2265G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454174 | ||||||
chr13:49454248
|
A | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0191 | 2 | HG01358.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.16+2339A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454248 | ||||||
chr13:49454251
|
T | A | 1 | a0001c0002t0013g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+2342T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454251 | ||||||
chr13:49454363
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 317 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.16+2454T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454363 | ||||||
chr13:49454553
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.16+2644G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454553 | ||||||
chr13:49454749
|
A | G | 1 | a0001c0014t0002g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.16+2840A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454749 | ||||||
chr13:49454900
|
C | T | 48 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+2991C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454900 | ||||||
chr13:49455145
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.16+3236C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455145 | ||||||
chr13:49455244
|
G | A | 48 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+3335G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455244 | ||||||
chr13:49455296
|
A | G | 1 | a0001c0001t0023g0132 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.16+3387A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455296 | ||||||
chr13:49455339
|
G | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 317 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.16+3430G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455339 | ||||||
chr13:49455446
|
C | T | 2 | a0003c0004t0018g0196a0003c0004t0018g0197 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.16+3537C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455446 | ||||||
chr13:49455462
|
G | T | 4 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+3553G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455462 | ||||||
chr13:49455527
|
T | G | 1 | a0001c0001t0016g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.16+3618T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455527 | ||||||
chr13:49455549
|
C | T | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16+3640C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455549 | ||||||
chr13:49455648
|
C | T | 48 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+3739C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455648 | ||||||
chr13:49455652
|
A | T | 1 | a0001c0002t0025g0375 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.16+3743A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455652 | ||||||
chr13:49455755
|
A | G | 1 | a0001c0002t0008g0371 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.16+3846A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455755 | ||||||
chr13:49455785
|
CAAAA | C | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.16+3882_16+3885del others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49455785 | |||||
chr13:49455805
|
TA | T | 8 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(5): Show | 10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+3897delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455805 | ||||||
chr13:49455840
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 317 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.16+3931T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455840 | ||||||
chr13:49455864
|
A | G | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+3955A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455864 | ||||||
chr13:49455909
|
G | A | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+4000G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455909 | ||||||
chr13:49455971
|
G | T | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.16+4062G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455971 | ||||||
chr13:49456032
|
G | A | 1 | a0001c0002t0022g0340 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.17-4075G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456032 | ||||||
chr13:49456129
|
C | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.17-3978C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456129 | ||||||
chr13:49456210
|
C | A | 4 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-3897C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456210 | ||||||
chr13:49456528
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.17-3579G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456528 | ||||||
chr13:49456566
|
G | T | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.17-3541G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456566 | ||||||
chr13:49456688
|
T | C | 3 | a0001c0002t0004g0015a0001c0002t0004g0265a0001c0002t0004g0266 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-3419T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456688 | ||||||
chr13:49456850
|
G | A | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.17-3257G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456850 | ||||||
chr13:49456892
|
G | A | 1 | a0003c0004t0005g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.17-3215G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456892 | ||||||
chr13:49456926
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.17-3181G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456926 | ||||||
chr13:49457034
|
G | T | 39 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(36): Show | 46 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-3073G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457034 | ||||||
chr13:49457215
|
C | CCT | 3 | a0001c0002t0004g0015a0001c0002t0004g0265a0001c0002t0004g0266 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2892_17-2891ins others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457215 | ||||||
chr13:49457215
|
C | CT | 9 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0379others(6): Show | 9 | HG01109.hp1 HG02015.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-2877dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457215 | |||||
chr13:49457215
|
C | CTT | 150 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(147): Show | 161 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.17-2878_17-2877dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457215 | |||||
chr13:49457216
|
T | TTC | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(156): Show | 168 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.17-2890_17-2889ins others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457216 | |||||
chr13:49457217
|
T | TC | 3 | a0001c0001t0001g0031a0001c0001t0001g0136a0001c0001t0010g0052 | 3 | HG02647.hp2 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.17-2890_17-2889ins others(1): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457217 | ||||||
chr13:49457261
|
G | A | 1 | a0003c0004t0005g0205 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.17-2846G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457261 | ||||||
chr13:49457287
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-2820T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457287 | ||||||
chr13:49457292
|
T | G | 1 | a0003c0004t0005g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17-2815T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457292 | ||||||
chr13:49457306
|
A | AT | 8 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(5): Show | 10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.17-2797dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457306 | |||||
chr13:49457400
|
A | AG | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(325): Show | 349 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(346): Show |
intron_variant | MODIFIER | c.17-2707_17-2706ins others(1): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457400 | ||||||
chr13:49457435
|
C | CT | 16 | a0001c0001t0001g0090a0002c0003t0003g0295a0002c0003t0003g0322others(13): Show | 17 | HG00280.hp1 HG00609.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.17-2654dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457435 | |||||
chr13:49457435
|
CT | C | 278 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(275): Show | 298 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.17-2654delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457435 | |||||
chr13:49457435
|
CTT | C | 8 | a0001c0001t0001g0136a0001c0001t0042g0137a0001c0002t0002g0248others(5): Show | 8 | HG01074.hp2 HG02897.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-2655_17-2654del others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457435 | |||||
chr13:49457470
|
G | A | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.17-2637G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457470 | ||||||
chr13:49457474
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 317 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.17-2633C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457474 | ||||||
chr13:49457591
|
G | A | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.17-2516G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457591 | ||||||
chr13:49457732
|
A | G | 105 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(102): Show | 109 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.17-2375A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457732 | ||||||
chr13:49457925
|
A | G | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.17-2182A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457925 | ||||||
chr13:49458157
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 169 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.17-1950C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458157 | ||||||
chr13:49458340
|
G | A | 63 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(60): Show | 64 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.17-1767G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458340 | ||||||
chr13:49458368
|
C | G | 1 | a0003c0004t0018g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.17-1739C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458368 | ||||||
chr13:49458463
|
C | T | 1 | a0004c0005t0006g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17-1644C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458463 | ||||||
chr13:49458653
|
G | T | 1 | a0003c0004t0005g0224 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.17-1454G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458653 | ||||||
chr13:49458719
|
G | A | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.17-1388G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458719 | ||||||
chr13:49458838
|
C | T | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.17-1269C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458838 | ||||||
chr13:49458960
|
G | A | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.17-1147G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458960 | ||||||
chr13:49458965
|
G | C | 49 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0004g0334others(46): Show | 50 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.17-1142G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458965 | ||||||
chr13:49458992
|
C | A | 2 | a0002c0003t0003g0307a0002c0003t0003g0327 | 2 | HG02056.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.17-1115C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458992 | ||||||
chr13:49459007
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.17-1100C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459007 | ||||||
chr13:49459052
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(145): Show | 156 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.17-1055G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459052 | ||||||
chr13:49459530
|
T | A | 3 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197 | 3 | HG01109.hp1 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.17-577T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459530 | ||||||
chr13:49459741
|
C | T | 5 | a0003c0004t0005g0203a0003c0004t0005g0207a0003c0004t0005g0222others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-366C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459741 | ||||||
chr13:49459767
|
T | C | 3 | a0001c0002t0004g0015a0001c0002t0004g0265a0001c0002t0004g0266 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-340T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459767 | ||||||
chr13:49459804
|
T | C | 11 | a0001c0002t0002g0001a0001c0002t0002g0232a0001c0002t0002g0233others(8): Show | 15 | NA18612.hp1 NA18946.hp2 NA18953.hp2 others(12): Show |
intron_variant | MODIFIER | c.17-303T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459804 | ||||||
chr13:49459894
|
A | T | 1 | a0001c0001t0016g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.17-213A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459894 | ||||||
chr13:49460001
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-106T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49460001 | ||||||
chr13:49460256
|
A | G | 2 | a0001c0002t0004g0344a0001c0002t0004g0346 | 2 | NA19060.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.142+24A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460256 | ||||||
chr13:49460261
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.142+29T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460261 | ||||||
chr13:49460548
|
C | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(160): Show | 172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.142+316C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460548 | ||||||
chr13:49460587
|
T | G | 8 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+355T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460587 | ||||||
chr13:49460606
|
G | C | 4 | a0004c0005t0006g0064a0004c0005t0006g0065a0004c0005t0006g0066others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+374G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460606 | ||||||
chr13:49460646
|
A | AT | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.142+420dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr13 | 49460646 | |||||
chr13:49460655
|
A | T | 1 | a0002c0003t0033g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.142+423A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460655 | ||||||
chr13:49460749
|
T | C | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-348T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460749 | ||||||
chr13:49460906
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 317 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.143-191T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460906 | ||||||
chr13:49460912
|
G | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 317 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.143-185G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460912 | ||||||
chr13:49461015
|
G | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.143-82G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49461015 | ||||||
chr13:49461072
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(160): Show | 172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.143-25G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49461072 | ||||||
chr13:49461276
|
T | G | 1 | a0001c0008t0005g0008 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.208+114T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461276 | ||||||
chr13:49461293
|
C | T | 30 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(27): Show | 31 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.208+131C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461293 | ||||||
chr13:49461377
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.208+215A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461377 | ||||||
chr13:49461398
|
G | A | 7 | a0001c0001t0010g0052a0001c0001t0010g0157a0001c0001t0010g0158others(4): Show | 7 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+236G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461398 | ||||||
chr13:49461660
|
G | A | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+498G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461660 | ||||||
chr13:49461944
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.208+782G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461944 | ||||||
chr13:49462216
|
T | C | 1 | a0002c0003t0003g0311 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.208+1054T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462216 | ||||||
chr13:49462262
|
C | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0088others(61): Show | 68 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+1100C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462262 | ||||||
chr13:49462426
|
T | C | 1 | a0001c0002t0029g0372 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+1264T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462426 | ||||||
chr13:49462546
|
C | A | 3 | a0001c0001t0016g0189a0001c0001t0044g0188a0001c0001t0045g0190 | 3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.208+1384C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462546 | ||||||
chr13:49462562
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.208+1400A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462562 | ||||||
chr13:49462574
|
T | C | 1 | a0001c0008t0005g0008 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.208+1412T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462574 | ||||||
chr13:49462654
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.208+1492A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462654 | ||||||
chr13:49462698
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0166 | 2 | HG02165.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.208+1536A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462698 | ||||||
chr13:49462731
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.208+1569C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462731 | ||||||
chr13:49463130
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 22 | HG00621.hp2 HG01975.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+1968C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463130 | ||||||
chr13:49463162
|
C | T | 2 | a0002c0003t0003g0307a0002c0003t0003g0327 | 2 | HG02056.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.208+2000C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463162 | ||||||
chr13:49463171
|
AT | A | 287 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(284): Show | 306 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.208+2021delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49463171 | |||||
chr13:49463186
|
A | G | 14 | a0001c0002t0007g0243a0001c0002t0007g0269a0001c0002t0007g0271others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+2024A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463186 | ||||||
chr13:49463290
|
C | T | 2 | a0001c0001t0005g0336a0001c0001t0005g0337 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.208+2128C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463290 | ||||||
chr13:49463369
|
G | A | 1 | a0001c0002t0012g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208+2207G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463369 | ||||||
chr13:49463531
|
T | C | 8 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2369T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463531 | ||||||
chr13:49463669
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.208+2507G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463669 | ||||||
chr13:49463727
|
C | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.208+2565C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463727 | ||||||
chr13:49463728
|
CACT | C | 7 | a0001c0002t0017g0011a0001c0002t0028g0228a0003c0004t0018g0195others(4): Show | 8 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2567_208+2569d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463728 | ||||||
chr13:49463777
|
G | T | 1 | a0001c0001t0016g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208+2615G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463777 | ||||||
chr13:49463820
|
T | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 183 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.208+2658T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463820 | ||||||
chr13:49463944
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 144 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.208+2782G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463944 | ||||||
chr13:49464073
|
C | T | 31 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0002t0004g0220others(28): Show | 32 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.208+2911C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464073 | ||||||
chr13:49464219
|
T | C | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+3057T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464219 | ||||||
chr13:49464221
|
C | T | 60 | a0001c0002t0004g0334a0001c0002t0004g0335a0001c0002t0004g0338others(57): Show | 61 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.208+3059C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464221 | ||||||
chr13:49464252
|
A | T | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.208+3090A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464252 | ||||||
chr13:49464284
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.208+3122T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464284 | ||||||
chr13:49464357
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.208+3195T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464357 | ||||||
chr13:49464394
|
C | G | 1 | a0001c0001t0044g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208+3232C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464394 | ||||||
chr13:49464521
|
C | T | 14 | a0001c0002t0007g0243a0001c0002t0007g0269a0001c0002t0007g0271others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-3343C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464521 | ||||||
chr13:49464531
|
C | T | 3 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0008t0005g0008 | 4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-3333C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464531 | ||||||
chr13:49464594
|
C | T | 1 | a0001c0014t0002g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.209-3270C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464594 | ||||||
chr13:49464704
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(293): Show | 316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.209-3160A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464704 | ||||||
chr13:49464981
|
G | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.209-2883G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464981 | ||||||
chr13:49465072
|
T | TA | 228 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(225): Show | 242 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.209-2778dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49465072 | |||||
chr13:49465115
|
A | T | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(292): Show | 315 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.209-2749A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465115 | ||||||
chr13:49465180
|
A | C | 8 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2684A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465180 | ||||||
chr13:49465211
|
T | C | 1 | a0002c0003t0014g0321 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.209-2653T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465211 | ||||||
chr13:49465237
|
G | A | 16 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(13): Show | 18 | HG01074.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2627G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465237 | ||||||
chr13:49465372
|
A | G | 32 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0002t0004g0220others(29): Show | 33 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.209-2492A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465372 | ||||||
chr13:49465539
|
A | AT | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0127others(3): Show | 6 | HG01517.hp1 HG01981.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-2311dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49465539 | |||||
chr13:49465600
|
G | A | 1 | a0003c0004t0005g0205 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.209-2264G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465600 | ||||||
chr13:49465629
|
C | T | 2 | a0001c0001t0001g0039a0002c0003t0033g0309 | 2 | HG02280.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.209-2235C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465629 | ||||||
chr13:49465662
|
G | A | 1 | a0001c0002t0007g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.209-2202G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465662 | ||||||
chr13:49465785
|
C | T | 10 | a0001c0002t0008g0019a0001c0002t0008g0020a0001c0002t0008g0366others(7): Show | 11 | HG00558.hp2 HG02132.hp1 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-2079C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465785 | ||||||
chr13:49466160
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.209-1704G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466160 | ||||||
chr13:49466254
|
G | C | 17 | a0001c0001t0001g0094a0001c0001t0001g0136a0001c0001t0001g0138others(14): Show | 17 | HG00438.hp1 HG02074.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.209-1610G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466254 | ||||||
chr13:49466438
|
T | TA | 36 | a0001c0001t0001g0138a0001c0001t0037g0100a0001c0002t0004g0220others(33): Show | 37 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.209-1410dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466438 | |||||
chr13:49466438
|
TA | T | 14 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0002t0004g0374others(11): Show | 15 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.209-1410delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466438 | |||||
chr13:49466457
|
T | G | 329 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(326): Show | 350 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.209-1407T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466457 | ||||||
chr13:49466573
|
G | A | 1 | a0002c0003t0003g0312 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.209-1291G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466573 | ||||||
chr13:49466684
|
G | A | 3 | a0001c0002t0004g0347a0001c0002t0004g0348a0001c0002t0004g0349 | 3 | HG02155.hp1 NA19009.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.209-1180G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466684 | ||||||
chr13:49466811
|
C | CT | 92 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(89): Show | 103 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.209-1033dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | |||||
chr13:49466811
|
C | CTT | 189 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 198 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.209-1034_209-1033d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | |||||
chr13:49466811
|
C | CTTT | 11 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0098others(8): Show | 11 | HG01123.hp2 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-1035_209-1033d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | |||||
chr13:49466811
|
CT | C | 29 | a0001c0002t0004g0220a0003c0004t0005g0010a0003c0004t0005g0199others(26): Show | 30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-1033delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | |||||
chr13:49466872
|
C | T | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.209-992C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466872 | ||||||
chr13:49467082
|
G | C | 1 | a0001c0001t0044g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.209-782G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467082 | ||||||
chr13:49467265
|
C | T | 46 | a0001c0002t0004g0334a0001c0002t0004g0335a0001c0002t0004g0338others(43): Show | 47 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.209-599C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467265 | ||||||
chr13:49467366
|
C | T | 2 | a0001c0001t0001g0122a0003c0004t0018g0195 | 2 | HG02895.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.209-498C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467366 | ||||||
chr13:49467398
|
CA | C | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.209-457delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49467398 | |||||
chr13:49467675
|
T | G | 1 | a0001c0002t0017g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.209-189T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467675 | ||||||
chr13:49467791
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.209-73A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467791 | ||||||
chr13:49467809
|
T | C | 1 | a0003c0004t0005g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-55T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467809 | ||||||
chr13:49467974
|
T | C | 1 | a0002c0003t0003g0294 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.305+14T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49467974 | ||||||
chr13:49468348
|
T | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(136): Show | 146 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.305+388T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468348 | ||||||
chr13:49468590
|
A | G | 8 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+630A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468590 | ||||||
chr13:49468594
|
T | C | 3 | a0001c0002t0020g0227a0001c0002t0020g0267a0001c0002t0020g0275 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+634T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468594 | ||||||
chr13:49468614
|
T | TGTTACCC others(309): Show |
1 | a0001c0014t0002g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.305+668_305+669ins others(316): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(319): Show |
1 | a0001c0002t0027g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.305+668_305+669ins others(326): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(319): Show |
12 | a0001c0002t0007g0243a0001c0002t0007g0269a0001c0002t0007g0271others(9): Show | 12 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(326): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(320): Show |
2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(327): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(322): Show |
3 | a0004c0005t0006g0064a0004c0005t0006g0065a0004c0005t0006g0066 | 3 | HG01243.hp1 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.305+668_305+669ins others(329): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(323): Show |
1 | a0004c0005t0006g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.305+668_305+669ins others(330): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(323): Show |
39 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(36): Show | 46 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(330): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(324): Show |
2 | a0001c0002t0002g0229a0001c0002t0002g0230 | 2 | HG01192.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(331): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(325): Show |
2 | a0001c0002t0004g0344a0001c0002t0004g0346 | 2 | NA19060.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.305+668_305+669ins others(332): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(326): Show |
37 | a0001c0002t0004g0334a0001c0002t0004g0335a0001c0002t0004g0338others(34): Show | 38 | HG00558.hp2 HG02015.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(333): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(327): Show |
17 | a0001c0002t0004g0220a0001c0002t0004g0347a0001c0002t0004g0348others(14): Show | 17 | HG00408.hp2 HG00642.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(334): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(328): Show |
1 | a0001c0002t0004g0339 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.305+668_305+669ins others(335): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(335): Show |
2 | a0001c0002t0004g0015a0001c0002t0004g0265 | 3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(342): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(336): Show |
1 | a0001c0002t0012g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.305+668_305+669ins others(343): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(337): Show |
2 | a0001c0002t0004g0266a0001c0002t0012g0016 | 3 | HG03453.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(344): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468614
|
T | TGTTACCC others(338): Show |
2 | a0001c0002t0012g0281a0001c0002t0012g0282 | 2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.305+668_305+669ins others(345): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | |||||
chr13:49468623
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.305+663A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468623 | ||||||
chr13:49468661
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.305+701A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468661 | ||||||
chr13:49468679
|
AT | A | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+726delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468679 | |||||
chr13:49468847
|
T | C | 47 | a0001c0002t0004g0220a0001c0002t0004g0334a0001c0002t0004g0335others(44): Show | 48 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.305+887T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468847 | ||||||
chr13:49469090
|
G | A | 28 | a0003c0004t0005g0010a0003c0004t0005g0199a0003c0004t0005g0200others(25): Show | 29 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.305+1130G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469090 | ||||||
chr13:49469156
|
C | T | 2 | a0001c0002t0002g0229a0001c0002t0002g0230 | 2 | HG01192.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.305+1196C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469156 | ||||||
chr13:49469278
|
C | T | 48 | a0001c0002t0004g0220a0001c0002t0004g0334a0001c0002t0004g0335others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.305+1318C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469278 | ||||||
chr13:49469500
|
T | C | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.305+1540T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469500 | ||||||
chr13:49469684
|
A | G | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.305+1724A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469684 | ||||||
chr13:49469874
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.305+1914C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469874 | ||||||
chr13:49469938
|
C | T | 1 | a0001c0002t0004g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.305+1978C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469938 | ||||||
chr13:49470420
|
C | G | 1 | a0001c0002t0004g0379 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.305+2460C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470420 | ||||||
chr13:49470449
|
T | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.305+2489T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470449 | ||||||
chr13:49470522
|
CTT | C | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+2563_305+2564d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470522 | ||||||
chr13:49470539
|
T | C | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.305+2579T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470539 | ||||||
chr13:49470574
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.305+2614A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470574 | ||||||
chr13:49470618
|
C | T | 1 | a0001c0002t0004g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.305+2658C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470618 | ||||||
chr13:49470619
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.305+2659A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470619 | ||||||
chr13:49470845
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(242): Show | 264 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.305+2885A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470845 | ||||||
chr13:49470847
|
A | G | 3 | a0001c0002t0020g0227a0001c0002t0020g0267a0001c0002t0020g0275 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+2887A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470847 | ||||||
chr13:49470861
|
A | G | 1 | a0001c0001t0009g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.305+2901A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470861 | ||||||
chr13:49470872
|
G | T | 1 | a0001c0001t0016g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305+2912G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470872 | ||||||
chr13:49470888
|
A | G | 1 | a0001c0002t0004g0365 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.305+2928A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470888 | ||||||
chr13:49470927
|
T | G | 1 | a0001c0001t0016g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305+2967T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470927 | ||||||
chr13:49470941
|
G | T | 3 | a0001c0002t0020g0227a0001c0002t0020g0267a0001c0002t0020g0275 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+2981G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470941 | ||||||
chr13:49470966
|
C | CT | 50 | a0002c0003t0003g0005a0002c0003t0003g0018a0002c0003t0003g0082others(47): Show | 54 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.305+3024dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTT | 20 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0050others(17): Show | 21 | HG00280.hp2 HG01243.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT | 71 | a0001c0002t0004g0334a0001c0002t0004g0338a0001c0002t0004g0341others(68): Show | 73 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT others(3): Show |
95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(92): Show | 100 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT others(4): Show |
18 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0094others(15): Show | 18 | HG00609.hp1 HG01123.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.305+3009_305+3010i others(16): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT others(1): Show |
38 | a0001c0001t0001g0155a0001c0001t0010g0158a0001c0001t0016g0058others(35): Show | 40 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT others(2): Show |
66 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(63): Show | 76 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(11): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470966
|
C | CTTTCTTT others(3): Show |
12 | a0001c0001t0001g0168a0001c0001t0009g0076a0001c0001t0009g0080others(9): Show | 13 | HG00597.hp1 HG01192.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | |||||
chr13:49470968
|
T | TTCTTTCT others(3): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.305+3009_305+3010i others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470968 | |||||
chr13:49471145
|
A | AT | 144 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 152 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.305+3197dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471145 | |||||
chr13:49471222
|
C | T | 2 | a0001c0002t0002g0260a0001c0002t0002g0261 | 2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.305+3262C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471222 | ||||||
chr13:49471276
|
C | T | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.305+3316C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471276 | ||||||
chr13:49471285
|
A | G | 28 | a0003c0004t0005g0010a0003c0004t0005g0199a0003c0004t0005g0200others(25): Show | 29 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.305+3325A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471285 | ||||||
chr13:49471350
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.305+3390A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471350 | ||||||
chr13:49471411
|
C | T | 16 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(13): Show | 18 | HG01074.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.305+3451C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471411 | ||||||
chr13:49471420
|
C | CT | 31 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0053others(28): Show | 33 | HG00621.hp2 HG00735.hp2 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.305+3477dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471420 | |||||
chr13:49471420
|
C | CTT | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+3476_305+3477d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471420 | |||||
chr13:49471420
|
CT | C | 69 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0049others(66): Show | 79 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.305+3477delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471420 | |||||
chr13:49471613
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.305+3653C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471613 | ||||||
chr13:49471828
|
AG | A | 14 | a0001c0002t0007g0243a0001c0002t0007g0269a0001c0002t0007g0271others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+3869delG | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471828 | ||||||
chr13:49471864
|
C | G | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+3904C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471864 | ||||||
chr13:49471913
|
C | CAT | 3 | a0001c0001t0016g0189a0001c0014t0002g0264a0002c0003t0007g0287 | 3 | HG00597.hp1 HG01884.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.305+3974_305+3975d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATAT | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG01346.hp1 HG02004.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.305+3970_305+3975d others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(1): Show |
3 | a0001c0001t0023g0119a0001c0002t0017g0011a0001c0002t0028g0228 | 4 | HG01257.hp1 HG01258.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+3968_305+3975d others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.305+3966_305+3975d others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(5): Show |
29 | a0001c0002t0004g0335a0001c0002t0004g0339a0001c0002t0004g0341others(26): Show | 30 | HG00642.hp1 HG02132.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.305+3964_305+3975d others(14): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(7): Show |
4 | a0001c0002t0004g0220a0001c0002t0004g0357a0001c0002t0004g0365others(1): Show | 4 | HG00408.hp2 HG02135.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+3962_305+3975d others(16): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(9): Show |
2 | a0001c0002t0008g0377a0003c0004t0018g0195 | 2 | HG00558.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.305+3960_305+3975d others(18): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(11): Show |
2 | a0001c0002t0004g0346a0001c0002t0004g0379 | 2 | HG02015.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.305+3958_305+3975d others(20): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471913
|
C | CATATATA others(13): Show |
2 | a0001c0002t0004g0344a0001c0002t0004g0360 | 2 | HG03688.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.305+3956_305+3975d others(22): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | |||||
chr13:49471926
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.305+3966A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471926 | ||||||
chr13:49471927
|
TATATATA | T | 9 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.305+3968_305+3974d others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471927 | ||||||
chr13:49471929
|
TA | T | 3 | a0001c0002t0020g0227a0001c0002t0020g0267a0001c0002t0020g0275 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+3970delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471929 | ||||||
chr13:49471930
|
A | AT | 5 | a0001c0001t0010g0052a0001c0001t0010g0158a0001c0001t0010g0169others(2): Show | 5 | HG01975.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+3971dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471930 | |||||
chr13:49471930
|
A | T | 2 | a0001c0001t0010g0157a0001c0001t0010g0192 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.305+3970A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471930 | ||||||
chr13:49471931
|
TA | T | 7 | a0001c0002t0007g0269a0001c0002t0007g0271a0001c0002t0007g0276others(4): Show | 7 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.305+3972delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471931 | ||||||
chr13:49471932
|
A | AT | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0156others(6): Show | 9 | HG00621.hp2 HG02165.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.305+3973dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471932 | |||||
chr13:49471932
|
A | ATTT | 3 | a0003c0004t0005g0202a0003c0004t0005g0217a0003c0004t0005g0231 | 3 | HG01257.hp2 HG02015.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.305+3973_305+3974i others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471932 | |||||
chr13:49471932
|
A | T | 10 | a0001c0001t0010g0052a0001c0001t0010g0157a0001c0001t0010g0158others(7): Show | 10 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.305+3972A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471932 | ||||||
chr13:49471933
|
TA | T | 6 | a0001c0002t0007g0243a0001c0002t0007g0273a0001c0002t0007g0274others(3): Show | 6 | HG00741.hp1 HG01106.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.305+3974delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471933 | ||||||
chr13:49471934
|
A | AT | 7 | a0001c0001t0001g0161a0001c0001t0024g0057a0001c0002t0002g0229others(4): Show | 7 | HG01192.hp2 HG02080.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.305+3989dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0004g0350 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.305+3975_305+3976i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0004g0359 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.305+3975_305+3976i others(15): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | ATATATAT others(5): Show |
3 | a0001c0002t0004g0334a0001c0002t0004g0338a0001c0002t0025g0375 | 3 | HG02027.hp1 HG02602.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.305+3975_305+3976i others(14): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0004g0362 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.305+3975_305+3976i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | ATATT | 8 | a0001c0001t0001g0155a0003c0004t0005g0203a0003c0004t0005g0204others(5): Show | 8 | HG02109.hp2 HG02132.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | ATTTT | 12 | a0003c0004t0005g0199a0003c0004t0005g0200a0003c0004t0005g0201others(9): Show | 12 | HG01109.hp2 HG02083.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.305+3986_305+3989d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471934
|
A | T | 36 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0156others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.305+3974A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471934 | ||||||
chr13:49471934
|
AT | A | 5 | a0001c0002t0004g0015a0001c0002t0004g0265a0001c0002t0004g0266others(2): Show | 7 | HG01070.hp1 HG01071.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.305+3989delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | |||||
chr13:49471935
|
T | TA | 39 | a0001c0001t0005g0337a0001c0001t0016g0058a0001c0001t0016g0061others(36): Show | 47 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATA | 27 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 29 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATA | 59 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 64 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATATA | 22 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0084others(19): Show | 22 | HG00609.hp1 HG01099.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATATA others(2): Show |
12 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0094others(9): Show | 12 | HG00621.hp1 HG01358.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(11): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATATA others(4): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0121others(4): Show | 7 | HG03704.hp2 HG04204.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATATA others(6): Show |
2 | a0001c0001t0001g0107a0001c0002t0027g0333 | 2 | HG02886.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.305+3975_305+3976i others(15): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATATA others(10): Show |
1 | a0003c0004t0021g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.305+3975_305+3976i others(19): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471935
|
T | TATATATA others(12): Show |
2 | a0003c0004t0018g0196a0007c0009t0021g0194 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.305+3975_305+3976i others(21): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | ||||||
chr13:49471936
|
T | A | 26 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(23): Show | 28 | HG00597.hp1 HG00642.hp1 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.305+3976T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471936 | ||||||
chr13:49471937
|
T | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(109): Show | 118 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.305+3977T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471937 | ||||||
chr13:49471938
|
T | A | 15 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(12): Show | 17 | HG01346.hp1 HG02004.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.305+3978T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471938 | ||||||
chr13:49471939
|
T | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0040others(48): Show | 53 | HG00438.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.305+3979T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471939 | ||||||
chr13:49471940
|
T | A | 6 | a0001c0001t0001g0086a0001c0001t0001g0104a0001c0001t0001g0186others(3): Show | 6 | HG02004.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.305+3980T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471940 | ||||||
chr13:49471941
|
T | A | 15 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0099others(12): Show | 15 | HG01168.hp1 HG02055.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.305+3981T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471941 | ||||||
chr13:49471942
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.305+3982T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471942 | ||||||
chr13:49472108
|
A | G | 1 | a0001c0002t0011g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.305+4148A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49472108 | ||||||
chr13:49472526
|
T | C | 1 | a0001c0002t0012g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.306-3950T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49472526 | ||||||
chr13:49472621
|
C | A | 1 | a0002c0003t0003g0298 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.306-3855C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49472621 | ||||||
chr13:49473301
|
G | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.306-3175G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473301 | ||||||
chr13:49473393
|
A | T | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.306-3083A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473393 | ||||||
chr13:49473419
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01346.hp1 HG02004.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.306-3057C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473419 | ||||||
chr13:49473444
|
G | A | 1 | a0001c0001t0023g0132 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.306-3032G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473444 | ||||||
chr13:49473485
|
A | G | 8 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(5): Show | 10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.306-2991A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473485 | ||||||
chr13:49473497
|
A | G | 1 | a0001c0002t0004g0365 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.306-2979A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473497 | ||||||
chr13:49473505
|
T | G | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-2971T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473505 | ||||||
chr13:49473551
|
C | CA | 45 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0032others(42): Show | 48 | HG00741.hp2 HG01192.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.306-2903dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | |||||
chr13:49473551
|
C | CAA | 64 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(61): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.306-2904_306-2903d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | |||||
chr13:49473551
|
C | CAAA | 22 | a0001c0002t0002g0237a0001c0002t0002g0256a0001c0002t0002g0260others(19): Show | 22 | HG00642.hp1 HG01952.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.306-2905_306-2903d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | |||||
chr13:49473551
|
CA | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0092others(5): Show | 8 | HG00140.hp1 HG01074.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.306-2903delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | |||||
chr13:49473845
|
G | A | 3 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0008t0005g0008 | 4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.306-2631G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473845 | ||||||
chr13:49473852
|
G | C | 1 | a0001c0002t0007g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.306-2624G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473852 | ||||||
chr13:49474019
|
T | C | 1 | a0003c0004t0005g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.306-2457T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474019 | ||||||
chr13:49474265
|
C | CA | 85 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(82): Show | 95 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.306-2201dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49474265 | |||||
chr13:49474354
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.306-2122T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474354 | ||||||
chr13:49474363
|
G | T | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-2113G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474363 | ||||||
chr13:49474444
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.306-2032C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474444 | ||||||
chr13:49474521
|
T | A | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-1955T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474521 | ||||||
chr13:49474614
|
G | A | 4 | a0004c0005t0006g0064a0004c0005t0006g0065a0004c0005t0006g0066others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-1862G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474614 | ||||||
chr13:49474698
|
G | A | 1 | a0001c0001t0041g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.306-1778G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474698 | ||||||
chr13:49474734
|
G | C | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.306-1742G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474734 | ||||||
chr13:49474839
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(161): Show | 173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.306-1637A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474839 | ||||||
chr13:49474839
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.306-1637A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474839 | ||||||
chr13:49475005
|
C | T | 3 | a0001c0002t0020g0227a0001c0002t0020g0267a0001c0002t0020g0275 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.306-1471C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475005 | ||||||
chr13:49475014
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.306-1462G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475014 | ||||||
chr13:49475241
|
G | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0171others(4): Show | 8 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.306-1235G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475241 | ||||||
chr13:49475491
|
A | AT | 8 | a0001c0001t0001g0107a0001c0001t0044g0188a0001c0002t0002g0230others(5): Show | 8 | HG01109.hp1 HG01192.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.306-972dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49475491 | |||||
chr13:49475608
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.306-868C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475608 | ||||||
chr13:49475651
|
T | C | 14 | a0001c0002t0007g0243a0001c0002t0007g0269a0001c0002t0007g0271others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-825T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475651 | ||||||
chr13:49475716
|
G | A | 1 | a0002c0003t0003g0299 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.306-760G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475716 | ||||||
chr13:49475747
|
C | T | 1 | a0001c0002t0008g0019 | 2 | NA19064.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.306-729C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475747 | ||||||
chr13:49475800
|
T | A | 4 | a0001c0002t0004g0379a0001c0002t0020g0227a0001c0002t0020g0267others(1): Show | 4 | HG02015.hp2 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-676T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475800 | ||||||
chr13:49476184
|
G | T | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.306-292G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49476184 | ||||||
chr13:49476232
|
G | A | 3 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0008t0005g0008 | 4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.306-244G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49476232 | ||||||
chr13:49476259
|
T | C | 1 | a0001c0002t0028g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306-217T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49476259 | ||||||
chr13:49477059
|
G | A | 2 | a0002c0003t0003g0322a0002c0003t0003g0323 | 2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.869+20G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477059 | ||||||
chr13:49477089
|
G | A | 1 | a0001c0002t0028g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+50G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477089 | ||||||
chr13:49477201
|
C | T | 1 | a0004c0005t0006g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.869+162C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477201 | ||||||
chr13:49477508
|
A | C | 1 | a0001c0002t0029g0372 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869+469A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477508 | ||||||
chr13:49477529
|
A | G | 8 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(5): Show | 10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.869+490A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477529 | ||||||
chr13:49477561
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.869+522A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477561 | ||||||
chr13:49477866
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.869+827A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477866 | ||||||
chr13:49478016
|
T | C | 2 | a0002c0003t0003g0322a0002c0003t0003g0323 | 2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.869+977T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478016 | ||||||
chr13:49478157
|
T | C | 2 | a0003c0004t0005g0199a0003c0004t0005g0200 | 2 | HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.869+1118T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478157 | ||||||
chr13:49478319
|
A | G | 62 | a0001c0002t0004g0220a0001c0002t0004g0334a0001c0002t0004g0335others(59): Show | 63 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.869+1280A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478319 | ||||||
chr13:49478363
|
G | A | 1 | a0001c0002t0002g0253 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.869+1324G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478363 | ||||||
chr13:49478523
|
A | G | 1 | a0001c0002t0004g0346 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.869+1484A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478523 | ||||||
chr13:49478548
|
C | T | 1 | a0001c0002t0011g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.869+1509C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478548 | ||||||
chr13:49478927
|
A | G | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.870-1292A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478927 | ||||||
chr13:49478992
|
G | A | 1 | a0001c0001t0040g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870-1227G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478992 | ||||||
chr13:49479051
|
A | G | 1 | a0001c0002t0011g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.870-1168A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479051 | ||||||
chr13:49479227
|
ATG | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.870-989_870-988del others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr13 | 49479227 | |||||
chr13:49479499
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.870-720A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479499 | ||||||
chr13:49479582
|
G | A | 3 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281 | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-637G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479582 | ||||||
chr13:49479599
|
C | T | 1 | a0002c0003t0007g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.870-620C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479599 | ||||||
chr13:49479740
|
G | A | 8 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(5): Show | 10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-479G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479740 | ||||||
chr13:49480017
|
A | G | 1 | a0001c0010t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.870-202A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480017 | ||||||
chr13:49480050
|
T | C | 1 | a0004c0005t0006g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.870-169T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480050 | ||||||
chr13:49480172
|
G | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.870-47G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480172 | ||||||
chr13:49480210
|
G | T | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.870-9G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480210 | ||||||
chr13:49480575
|
C | T | 4 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+240C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480575 | ||||||
chr13:49480611
|
G | A | 1 | a0001c0001t0045g0190 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.986+276G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480611 | ||||||
chr13:49480658
|
A | G | 3 | a0001c0002t0004g0015a0001c0002t0004g0265a0001c0002t0004g0266 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-289A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480658 | ||||||
chr13:49480702
|
A | G | 1 | a0001c0001t0044g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.987-245A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480702 | ||||||
chr13:49480823
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.987-124G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480823 | ||||||
chr13:49481296
|
G | A | 1 | a0001c0001t0045g0190 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1156+180G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481296 | ||||||
chr13:49481436
|
T | TA | 16 | a0001c0002t0004g0357a0001c0002t0004g0359a0002c0003t0003g0285others(13): Show | 16 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1156+331dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr13 | 49481436 | |||||
chr13:49481437
|
A | G | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1156+321A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481437 | ||||||
chr13:49481547
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0089a0001c0001t0001g0099others(4): Show | 7 | HG00733.hp1 HG01168.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156+431T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481547 | ||||||
chr13:49481748
|
A | G | 4 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156+632A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481748 | ||||||
chr13:49481837
|
A | AG | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1156+721_1156+722i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481837 | ||||||
chr13:49481864
|
G | T | 8 | a0001c0002t0002g0001a0001c0002t0002g0233a0001c0002t0002g0240others(5): Show | 12 | NA18612.hp1 NA18953.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.1156+748G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481864 | ||||||
chr13:49482001
|
G | A | 8 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157-736G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482001 | ||||||
chr13:49482149
|
G | A | 1 | a0002c0003t0014g0321 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1157-588G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482149 | ||||||
chr13:49482265
|
G | A | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157-472G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482265 | ||||||
chr13:49482265
|
G | C | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1157-472G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482265 | ||||||
chr13:49482657
|
T | C | 34 | a0003c0004t0005g0010a0003c0004t0005g0199a0003c0004t0005g0200others(31): Show | 35 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.1157-80T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482657 | ||||||
chr13:49483015
|
G | T | 6 | a0001c0001t0009g0077a0001c0001t0009g0079a0001c0002t0012g0016others(3): Show | 7 | HG02818.hp1 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+53G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483015 | ||||||
chr13:49483151
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1382+189A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483151 | ||||||
chr13:49483210
|
T | C | 8 | a0001c0001t0016g0058a0001c0001t0016g0059a0001c0001t0016g0061others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1382+248T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483210 | ||||||
chr13:49483269
|
T | C | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1383-195T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483269 | ||||||
chr13:49483276
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1383-188A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483276 | ||||||
chr13:49483380
|
G | A | 1 | a0005c0006t0002g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1383-84G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483380 | ||||||
chr13:49483609
|
A | AT | 22 | a0002c0003t0003g0005a0002c0003t0003g0285a0002c0003t0003g0299others(19): Show | 25 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1482+83dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
A | ATT | 13 | a0002c0003t0003g0083a0002c0003t0003g0284a0002c0003t0003g0296others(10): Show | 13 | HG01123.hp1 HG01934.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1482+82_1482+83dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTT | A | 8 | a0001c0002t0004g0360a0001c0002t0027g0333a0003c0004t0005g0204others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+78_1482+83del others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT | A | 58 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0041others(55): Show | 59 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1482+77_1482+83del others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT others(1): Show |
A | 130 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(127): Show | 136 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1482+76_1482+83del others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT others(2): Show |
A | 62 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0029others(59): Show | 67 | HG00280.hp2 HG00735.hp2 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.1482+75_1482+83del others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT others(3): Show |
A | 45 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0053others(42): Show | 53 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1482+74_1482+83del others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT others(4): Show |
A | 19 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0017g0163others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1482+73_1482+83del others(11): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT others(10): Show |
A | 3 | a0001c0002t0012g0016a0001c0002t0012g0280a0001c0002t0012g0281 | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+67_1482+83del others(17): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483609
|
ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0012g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1482+66_1482+83del others(18): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | |||||
chr13:49483728
|
G | A | 1 | a0002c0003t0003g0328 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1482+165G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49483728 | ||||||
chr13:49483800
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1482+237A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49483800 | ||||||
chr13:49483860
|
C | T | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1482+297C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49483860 | ||||||
chr13:49483974
|
AAATGTTT others(10): Show |
A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1482+413_1482+429d others(19): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483974 | |||||
chr13:49484034
|
G | A | 1 | a0001c0010t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1482+471G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484034 | ||||||
chr13:49484266
|
T | G | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1482+703T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484266 | ||||||
chr13:49484409
|
A | G | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1482+846A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484409 | ||||||
chr13:49484422
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1482+859A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484422 | ||||||
chr13:49484530
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1482+967G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484530 | ||||||
chr13:49484549
|
C | T | 2 | a0001c0002t0017g0011a0001c0002t0028g0228 | 3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1482+986C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484549 | ||||||
chr13:49484550
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(123): Show | 132 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1482+987G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484550 | ||||||
chr13:49484696
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1483-934T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484696 | ||||||
chr13:49484702
|
G | A | 15 | a0001c0002t0017g0011a0001c0002t0028g0228a0003c0004t0005g0201others(12): Show | 16 | HG01109.hp2 HG01257.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1483-928G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484702 | ||||||
chr13:49484731
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1483-899A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484731 | ||||||
chr13:49484942
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1483-688T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484942 | ||||||
chr13:49485218
|
C | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1483-412C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485218 | ||||||
chr13:49485395
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1483-235T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485395 | ||||||
chr13:49485520
|
C | T | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1483-110C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485520 | ||||||
chr13:49485535
|
T | C | 15 | a0003c0004t0005g0010a0003c0004t0005g0199a0003c0004t0005g0200others(12): Show | 16 | HG01257.hp2 HG02015.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1483-95T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485535 | ||||||
chr13:49485788
|
C | G | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1576+65C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49485788 | ||||||
chr13:49486030
|
TA | T | 14 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0064others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1576+310delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486030 | |||||
chr13:49486033
|
A | G | 1 | a0001c0002t0028g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1576+310A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486033 | ||||||
chr13:49486063
|
G | A | 1 | a0001c0002t0002g0246 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1576+340G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486063 | ||||||
chr13:49486281
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00438.hp2 NA18960.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576+558G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486281 | ||||||
chr13:49486303
|
C | CA | 39 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(36): Show | 42 | HG00621.hp2 HG01074.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1576+591dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486303 | |||||
chr13:49486303
|
C | CAA | 126 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(123): Show | 130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1576+590_1576+591d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486303 | |||||
chr13:49486303
|
C | CAAA | 71 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(68): Show | 82 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1576+589_1576+591d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486303 | |||||
chr13:49486310
|
A | AAT | 56 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0039others(53): Show | 58 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1576+588_1576+589i others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486310 | |||||
chr13:49486310
|
A | T | 1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1576+587A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486310 | ||||||
chr13:49486333
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1576+610G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486333 | ||||||
chr13:49486402
|
G | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1576+679G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486402 | ||||||
chr13:49486510
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1576+787A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486510 | ||||||
chr13:49486540
|
T | G | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.1576+817T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486540 | ||||||
chr13:49486568
|
T | C | 1 | a0002c0003t0003g0312 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1576+845T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486568 | ||||||
chr13:49486613
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1576+890G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486613 | ||||||
chr13:49486666
|
C | T | 1 | a0003c0004t0018g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1576+943C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486666 | ||||||
chr13:49486674
|
A | G | 1 | a0001c0002t0027g0333 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1576+951A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486674 | ||||||
chr13:49486842
|
G | A | 1 | a0001c0002t0002g0258 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1576+1119G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486842 | ||||||
chr13:49486984
|
T | C | 3 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0008t0005g0008 | 4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576+1261T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486984 | ||||||
chr13:49487075
|
G | A | 4 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0007g0273others(1): Show | 4 | HG00741.hp1 HG01993.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577-1215G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487075 | ||||||
chr13:49487136
|
G | A | 1 | a0001c0002t0022g0340 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1577-1154G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487136 | ||||||
chr13:49487376
|
C | T | 1 | a0001c0001t0017g0163 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1577-914C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487376 | ||||||
chr13:49487514
|
A | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 313 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.1577-776A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487514 | ||||||
chr13:49487675
|
T | A | 2 | a0001c0002t0004g0334a0001c0002t0004g0338 | 2 | HG02027.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1577-615T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487675 | ||||||
chr13:49487706
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1577-584C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487706 | ||||||
chr13:49487709
|
T | C | 9 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(6): Show | 11 | HG01106.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1577-581T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487709 | ||||||
chr13:49487974
|
T | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1577-316T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487974 | ||||||
chr13:49488037
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1577-253G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49488037 | ||||||
chr13:49488191
|
C | T | 326 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 347 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(344): Show |
intron_variant | MODIFIER | c.1577-99C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49488191 | ||||||
chr13:49488222
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1577-68G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49488222 | ||||||
chr13:49488686
|
T | G | 1 | a0001c0001t0016g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1917+56T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488686 | ||||||
chr13:49488775
|
T | C | 14 | a0001c0002t0007g0243a0001c0002t0007g0269a0001c0002t0007g0271others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1917+145T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488775 | ||||||
chr13:49488812
|
A | G | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1917+182A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488812 | ||||||
chr13:49488823
|
A | T | 48 | a0001c0002t0004g0220a0001c0002t0004g0334a0001c0002t0004g0335others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.1917+193A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488823 | ||||||
chr13:49488831
|
C | T | 3 | a0001c0002t0004g0015a0001c0002t0004g0265a0001c0002t0004g0266 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1917+201C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488831 | ||||||
chr13:49489102
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1917+472C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489102 | ||||||
chr13:49489165
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1917+535A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489165 | ||||||
chr13:49489189
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(101): Show | 108 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1917+559C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489189 | ||||||
chr13:49489224
|
C | T | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(60): Show | 72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1917+594C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489224 | ||||||
chr13:49489318
|
C | G | 4 | a0001c0002t0004g0345a0001c0002t0004g0352a0001c0002t0004g0354others(1): Show | 4 | NA18942.hp1 NA18943.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1917+688C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489318 | ||||||
chr13:49489375
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(288): Show | 311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1917+745G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489375 | ||||||
chr13:49489497
|
T | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1917+867T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489497 | ||||||
chr13:49489502
|
T | TA | 29 | a0001c0001t0001g0055a0001c0001t0001g0113a0001c0001t0010g0052others(26): Show | 33 | HG00408.hp1 HG01884.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1917+888dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489502 | |||||
chr13:49489512
|
A | G | 4 | a0004c0005t0006g0064a0004c0005t0006g0065a0004c0005t0006g0066others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1917+882A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489512 | ||||||
chr13:49489551
|
C | G | 293 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 313 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.1917+921C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489551 | ||||||
chr13:49489596
|
C | CT | 37 | a0001c0001t0001g0099a0001c0001t0001g0111a0001c0001t0001g0140others(34): Show | 38 | HG01069.hp2 HG01109.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1917+985dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489596 | |||||
chr13:49489596
|
C | CTT | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(209): Show | 231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1917+984_1917+985d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489596 | |||||
chr13:49489596
|
C | CTTT | 77 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0084others(74): Show | 78 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1917+983_1917+985d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489596 | |||||
chr13:49489621
|
C | T | 46 | a0001c0002t0004g0220a0001c0002t0004g0334a0001c0002t0004g0335others(43): Show | 47 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1917+991C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489621 | ||||||
chr13:49489643
|
C | T | 7 | a0001c0001t0001g0056a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG00609.hp1 HG01255.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1917+1013C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489643 | ||||||
chr13:49489665
|
C | T | 70 | a0001c0002t0004g0220a0001c0002t0004g0334a0001c0002t0004g0335others(67): Show | 73 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1917+1035C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489665 | ||||||
chr13:49489675
|
C | T | 1 | a0001c0008t0005g0008 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1917+1045C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489675 | ||||||
chr13:49489714
|
G | C | 10 | a0004c0005t0006g0022a0004c0005t0006g0063a0004c0005t0006g0068others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1917+1084G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489714 | ||||||
chr13:49489738
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 180 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1918-1084G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489738 | ||||||
chr13:49489769
|
C | T | 1 | a0001c0002t0002g0258 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1918-1053C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489769 | ||||||
chr13:49489842
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1918-980T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489842 | ||||||
chr13:49489886
|
G | A | 2 | a0001c0001t0040g0115a0001c0002t0020g0227 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1918-936G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489886 | ||||||
chr13:49489906
|
C | T | 5 | a0003c0004t0018g0195a0003c0004t0018g0196a0003c0004t0018g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1918-916C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489906 | ||||||
chr13:49489907
|
G | GC | 53 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(50): Show | 58 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1918-904dupC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489907 | |||||
chr13:49489907
|
G | GCC | 17 | a0001c0001t0016g0058a0001c0001t0016g0061a0001c0001t0019g0026others(14): Show | 17 | HG01243.hp2 HG02056.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1918-905_1918-904d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489907 | |||||
chr13:49489907
|
GC | G | 49 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0225others(46): Show | 57 | HG00408.hp1 HG01081.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.1918-904delC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489907 | |||||
chr13:49489918
|
C | CCCT | 25 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(22): Show | 26 | HG00280.hp2 HG00735.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.1918-904_1918-903i others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489918 | ||||||
chr13:49489918
|
C | CCT | 33 | a0001c0001t0010g0157a0002c0003t0003g0018a0002c0003t0003g0082others(30): Show | 34 | HG00140.hp2 HG01071.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1918-904_1918-903i others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489918 | ||||||
chr13:49489918
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0093others(22): Show | 27 | HG00438.hp2 HG00597.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1918-904C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489918 | ||||||
chr13:49489919
|
T | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(61): Show | 67 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1918-903T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489919 | ||||||
chr13:49489927
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0029others(26): Show | 32 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1918-895T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489927 | ||||||
chr13:49489927
|
T | TC | 35 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0046others(32): Show | 35 | HG00609.hp1 HG00639.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1918-895_1918-894i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489927 | ||||||
chr13:49489928
|
T | C | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(283): Show | 305 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.1918-894T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489928 | ||||||
chr13:49489928
|
T | TC | 30 | a0001c0001t0005g0337a0001c0002t0008g0368a0001c0002t0008g0370others(27): Show | 33 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1918-894_1918-893i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489928 | ||||||
chr13:49489928
|
T | TCC | 63 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(60): Show | 66 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1918-894_1918-893i others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489928 | ||||||
chr13:49489949
|
T | C | 39 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0001t0009g0062others(36): Show | 40 | HG01106.hp1 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1918-873T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489949 | ||||||
chr13:49490095
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1918-727G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490095 | ||||||
chr13:49490137
|
G | A | 36 | a0001c0001t0005g0336a0001c0001t0005g0337a0003c0004t0005g0010others(33): Show | 37 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.1918-685G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490137 | ||||||
chr13:49490279
|
C | CA | 27 | a0001c0002t0002g0248a0001c0002t0004g0334a0001c0002t0004g0335others(24): Show | 28 | HG00408.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1918-520dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
C | CAA | 60 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0155others(57): Show | 69 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1918-521_1918-520d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
C | CAAA | 39 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0095others(36): Show | 41 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1918-522_1918-520d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
C | CAAAA | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(82): Show | 91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1918-523_1918-520d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
C | CAAAAA | 47 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1918-524_1918-520d others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
C | CAAAAAA | 11 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0094others(8): Show | 12 | HG00558.hp1 HG00741.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1918-525_1918-520d others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
C | CAAAAAAA others(9): Show |
1 | a0003c0004t0030g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1918-535_1918-520d others(18): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490279
|
CAAAA | C | 28 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0002g0229others(25): Show | 29 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1918-523_1918-520d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | |||||
chr13:49490571
|
G | A | 2 | a0002c0003t0003g0082a0002c0003t0003g0083 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1918-251G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490571 | ||||||
chr13:49490579
|
T | C | 1 | a0002c0003t0033g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1918-243T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490579 | ||||||
chr13:49490703
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(288): Show | 310 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1918-119G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490703 | ||||||
chr13:49490792
|
C | T | 2 | a0001c0002t0028g0228a0002c0003t0033g0309 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1918-30C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490792 | ||||||
chr13:49490926
|
C | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 15 | HG00621.hp2 HG02165.hp2 HG03490.hp2 others(12): Show |
intron_variant | MODIFIER | c.2006+16C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49490926 | ||||||
chr13:49490947
|
G | A | 41 | a0001c0001t0005g0336a0001c0001t0005g0337a0001c0002t0012g0016others(38): Show | 44 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2006+37G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49490947 | ||||||
chr13:49491053
|
G | C | 1 | a0002c0003t0033g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2006+143G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491053 | ||||||
chr13:49491074
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(288): Show | 310 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.2006+164G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491074 | ||||||
chr13:49491341
|
A | G | 8 | a0001c0001t0009g0003a0001c0001t0009g0062a0001c0001t0009g0076others(5): Show | 10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2007-391A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491341 | ||||||
chr13:49491522
|
G | A | 1 | a0002c0003t0033g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2007-210G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491522 |