geneid | 23595 |
---|---|
ensemblid | ENSG00000135336.16 |
hgncid | 8489 |
symbol | ORC3 |
name | origin recognition complex subunit 3 |
refseq_nuc | NM_012381.4 |
refseq_prot | NP_036513.2 |
ensembl_nuc | ENST00000392844.8 |
ensembl_prot | ENSP00000376586.3 |
mane_status | MANE Select |
chr | chr6 |
start | 87590135 |
end | 87667451 |
strand | + |
ver | v1.2 |
region | chr6:87590135-87667451 |
region5000 | chr6:87585135-87672451 |
regionname0 | ORC3_chr6_87590135_87667451 |
regionname5000 | ORC3_chr6_87585135_87672451 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 711 | 357 | 82 | 69 | 152 | 14 | 38 | 122 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0002 | 0/0 | 711 | 9 | 1 | 3 | 3 | 1 | 1 | 3 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0003 | 0/0 | 711 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0004 | 0/0 | 711 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0005 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0006 | 0/0 | 711 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0007 | 0/0 | 711 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0008 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0009 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0010 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2136 | 342 | 68 | 69 | 152 | 14 | 37 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0002 | 0/0 | 2136 | 11 | 11 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0003 | 0/0 | 2136 | 9 | 1 | 3 | 3 | 1 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0004 | 0/0 | 2136 | 4 | 4 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0005 | 0/0 | 2136 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0006 | 0/0 | 2136 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0007 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0008 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0009 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0010 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0011 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0012 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
c0013 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
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 | 1/1 | 363 | 341 | 63 | 68 | 155 | 15 | 38 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
t0002 | 0/0 | 363 | 22 | 22 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
t0003 | 0/0 | 363 | 9 | 1 | 3 | 3 | 1 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
t0004 | 0/0 | 363 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
t0005 | 0/0 | 363 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
t0006 | 0/0 | 363 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
t0007 | 0/0 | 363 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0008 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2136 | 342 | 68 | 69 | 152 | 14 | 37 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0002 | 0/0 | 2136 | 11 | 11 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0005 | 0/0 | 2136 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0008 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0002c0003 | 0/0 | 2136 | 9 | 1 | 3 | 3 | 1 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0003c0004 | 0/0 | 2136 | 4 | 4 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0004c0006 | 0/0 | 2136 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0005c0012 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0006c0009 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0007c0010 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0008c0011 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0009c0013 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0010c0007 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2498 | 318 | 46 | 68 | 152 | 14 | 36 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0001t0002 | 0/0 | 2498 | 19 | 19 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0001t0004 | 0/0 | 2498 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0001t0005 | 0/0 | 2498 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0001t0007 | 0/0 | 2498 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0002t0001 | 0/0 | 2498 | 11 | 11 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0005t0002 | 0/0 | 2498 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0001c0008t0001 | 0/0 | 2498 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0002c0003t0003 | 0/0 | 2498 | 9 | 1 | 3 | 3 | 1 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0003c0004t0001 | 0/0 | 2498 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0003c0004t0006 | 0/0 | 2498 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0004c0006t0001 | 0/0 | 2498 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0005c0012t0001 | 0/0 | 2498 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0006c0009t0001 | 0/0 | 2498 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0007c0010t0001 | 0/0 | 2498 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0008c0011t0001 | 0/0 | 2498 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0009c0013t0001 | 0/0 | 2498 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
a0010c0007t0001 | 0/0 | 2498 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | copy fasta | chr6 | 87585135 | 87672451 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0005t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0005t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0005t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0001c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0002c0003t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0003c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0003c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0003c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0003c0004t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0004c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0004c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0005c0012t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0006c0009t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0007c0010t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0008c0011t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0009c0013t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
a0010c0007t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00140 | hp2 | a0006 | c0009 | t0001 | g0190 | EUR | GBR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00323 | hp1 | a0002 | c0003 | t0003 | g0347 | EUR | FIN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01256 | hp2 | a0002 | c0003 | t0003 | g0349 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01433 | hp1 | a0002 | c0003 | t0003 | g0351 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02145 | hp1 | a0002 | c0003 | t0003 | g0343 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CDX | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02258 | hp2 | a0003 | c0004 | t0001 | g0230 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02300 | hp2 | a0002 | c0003 | t0003 | g0348 | AMR | PEL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02615 | hp1 | a0001 | c0005 | t0002 | g0276 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02622 | hp1 | a0001 | c0005 | t0002 | g0277 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02622 | hp2 | a0003 | c0004 | t0001 | g0146 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02698 | hp1 | a0001 | c0008 | t0001 | g0039 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0032 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02922 | hp1 | a0003 | c0004 | t0006 | g0231 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02970 | hp2 | a0010 | c0007 | t0001 | g0352 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03209 | hp1 | a0009 | c0013 | t0001 | g0337 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03669 | hp1 | a0002 | c0003 | t0003 | g0350 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04115 | hp2 | a0007 | c0010 | t0001 | g0208 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | YRI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | YRI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0229 | AFR | YRI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18947 | hp2 | a0002 | c0003 | t0003 | g0344 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18990 | hp2 | a0004 | c0006 | t0001 | g0043 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19000 | hp2 | a0004 | c0006 | t0001 | g0044 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19010 | hp1 | a0002 | c0003 | t0003 | g0346 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0341 | AFR | LWK | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19064 | hp2 | a0002 | c0003 | t0003 | g0345 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19065 | hp2 | a0008 | c0011 | t0001 | g0187 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | YRI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20129 | hp1 | a0001 | c0005 | t0002 | g0278 | AFR | ASW | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ASW | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | GIH | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0342 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02486 | hp1 | a0005 | c0012 | t0001 | g0281 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | USA | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0340 | AFR | USA | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | LWK | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | LWK | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0254 | REF | REF | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0046 | REF | REF | ORC3_chr6_87585135_87672451 | ORC3 | chr6 | 87585135 | 87672451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:87594377
|
T | A | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.49T>A | p.Ser17Thr | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/20 | 83/2498 | 49/2136 | 17/711 | chr6 | 87594377 | ||
chr6:87603486
|
C | A | 1 | a0003 | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.280C>A | p.Gln94Lys | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/20 | 314/2498 | 280/2136 | 94/711 | chr6 | 87603486 | ||
chr6:87605971
|
A | G | 1 | a0009 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.377A>G | p.Gln126Arg | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/20 | 411/2498 | 377/2136 | 126/711 | chr6 | 87605971 | ||
chr6:87607793
|
C | T | 1 | a0005 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.548C>T | p.Ser183Leu | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/20 | 582/2498 | 548/2136 | 183/711 | chr6 | 87607793 | ||
chr6:87609165
|
G | A | 1 | a0002 | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
missense_variant | MODERATE | c.649G>A | p.Val217Ile | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/20 | 683/2498 | 649/2136 | 217/711 | chr6 | 87609165 | ||
chr6:87612157
|
G | A | 1 | a0004 | 2 | NA18990.hp2 NA19000.hp2 |
missense_variant | MODERATE | c.782G>A | p.Arg261Gln | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/20 | 816/2498 | 782/2136 | 261/711 | chr6 | 87612157 | ||
chr6:87621360
|
C | G | 1 | a0008 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.994C>G | p.Leu332Val | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 10/20 | 1028/2498 | 994/2136 | 332/711 | chr6 | 87621360 | ||
chr6:87653138
|
A | G | 1 | a0007 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1405A>G | p.Met469Val | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/20 | 1439/2498 | 1405/2136 | 469/711 | chr6 | 87653138 | ||
chr6:87667023
|
G | A | 1 | a0006 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.2036G>A | p.Arg679Gln | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 2070/2498 | 2036/2136 | 679/711 | chr6 | 87667023 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:87603482
|
C | G | 1 | a0001c0005 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.276C>G | p.Gly92Gly | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/20 | 310/2498 | 276/2136 | 92/711 | chr6 | 87603482 | ||
chr6:87621986
|
G | A | 1 | a0001c0008 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1158G>A | p.Ala386Ala | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/20 | 1192/2498 | 1158/2136 | 386/711 | chr6 | 87621986 | ||
chr6:87653225
|
C | T | 3 | a0001c0002a0002c0003a0005c0012 | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
synonymous_variant | LOW | c.1492C>T | p.Leu498Leu | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/20 | 1526/2498 | 1492/2136 | 498/711 | chr6 | 87653225 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:87667133
|
A | G | 1 | a0001c0001t0007 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 10 | chr6 | 87667133 | |||||
chr6:87667206
|
C | G | 2 | a0001c0001t0002a0001c0005t0002 | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*83C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 83 | chr6 | 87667206 | |||||
chr6:87667208
|
T | A | 1 | a0001c0001t0005 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 85 | chr6 | 87667208 | |||||
chr6:87667228
|
T | C | 2 | a0001c0001t0002a0001c0005t0002 | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 105 | chr6 | 87667228 | |||||
chr6:87667331
|
T | C | 1 | a0002c0003t0003 | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*208T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 208 | chr6 | 87667331 | |||||
chr6:87667335
|
A | T | 1 | a0003c0004t0006 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*212A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 212 | chr6 | 87667335 | |||||
chr6:87667425
|
A | G | 1 | a0001c0001t0004 | 3 | HG02976.hp2 NA18522.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*302A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 20/20 | 302 | chr6 | 87667425 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:87590295
|
A | G | 247 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(244): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.24+103A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590295 | ||||||
chr6:87590416
|
T | A | 165 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.24+224T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590416 | ||||||
chr6:87590514
|
A | G | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.24+322A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590514 | ||||||
chr6:87590785
|
A | G | 3 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355 | 3 | HG00597.hp1 NA19003.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.24+593A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590785 | ||||||
chr6:87590816
|
T | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.24+624T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590816 | ||||||
chr6:87590865
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA18944.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.24+673A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590865 | ||||||
chr6:87590908
|
G | A | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.24+716G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590908 | ||||||
chr6:87590909
|
A | G | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.24+717A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87590909 | ||||||
chr6:87591389
|
TA | T | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.24+1198delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87591389 | ||||||
chr6:87591403
|
C | CT | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.24+1215dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 87591403 | |||||
chr6:87591449
|
A | G | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.24+1257A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87591449 | ||||||
chr6:87591644
|
A | G | 5 | a0002c0003t0003g0347a0002c0003t0003g0348a0002c0003t0003g0349others(2): Show | 5 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+1452A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87591644 | ||||||
chr6:87591892
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.24+1700C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87591892 | ||||||
chr6:87591988
|
C | T | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.24+1796C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87591988 | ||||||
chr6:87592068
|
G | A | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.24+1876G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592068 | ||||||
chr6:87592287
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.25-2066C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592287 | ||||||
chr6:87592288
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.25-2065T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592288 | ||||||
chr6:87592289
|
A | T | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.25-2064A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592289 | ||||||
chr6:87592530
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.25-1823G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592530 | ||||||
chr6:87592716
|
T | G | 1 | a0001c0001t0001g0018 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.25-1637T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592716 | ||||||
chr6:87592729
|
G | A | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.25-1624G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592729 | ||||||
chr6:87592801
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | NA18953.hp2 NA18989.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.25-1552G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592801 | ||||||
chr6:87592816
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.25-1537G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87592816 | ||||||
chr6:87593080
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.25-1273G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593080 | ||||||
chr6:87593116
|
A | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0338a0001c0001t0001g0339 | 4 | HG01168.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1237A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593116 | ||||||
chr6:87593188
|
T | C | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.25-1165T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593188 | ||||||
chr6:87593345
|
C | T | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25-1008C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593345 | ||||||
chr6:87593372
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.25-981C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593372 | ||||||
chr6:87593404
|
G | A | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25-949G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593404 | ||||||
chr6:87593948
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.25-405G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593948 | ||||||
chr6:87593984
|
T | C | 247 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(244): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.25-369T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87593984 | ||||||
chr6:87594037
|
G | C | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.25-316G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87594037 | ||||||
chr6:87594249
|
A | C | 247 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(244): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.25-104A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87594249 | ||||||
chr6:87594261
|
A | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.25-92A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87594261 | ||||||
chr6:87594330
|
G | A | 26 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 26 | HG00544.hp2 HG00597.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.25-23G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87594330 | ||||||
chr6:87594337
|
G | A | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.25-16G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87594337 | ||||||
chr6:87594342
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.25-11T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 1/19 | chr6 | 87594342 | ||||||
chr6:87594413
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.79+6G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87594413 | ||||||
chr6:87594713
|
T | G | 2 | a0001c0001t0001g0353a0001c0001t0001g0354 | 2 | HG00597.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.79+306T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87594713 | ||||||
chr6:87594736
|
G | T | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.79+329G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87594736 | ||||||
chr6:87594908
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG01070.hp2 HG01123.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+501A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87594908 | ||||||
chr6:87595011
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.79+604A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595011 | ||||||
chr6:87595044
|
A | G | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(118): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.79+637A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595044 | ||||||
chr6:87595061
|
G | A | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.79+654G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595061 | ||||||
chr6:87595171
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 5 | HG01257.hp1 HG01943.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+764G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595171 | ||||||
chr6:87595361
|
A | G | 50 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 54 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.79+954A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595361 | ||||||
chr6:87595400
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.79+993T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595400 | ||||||
chr6:87595407
|
T | C | 43 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(40): Show | 43 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.79+1000T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595407 | ||||||
chr6:87595502
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.79+1095G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595502 | ||||||
chr6:87595660
|
A | G | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+1253A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595660 | ||||||
chr6:87595722
|
A | G | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.79+1315A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595722 | ||||||
chr6:87595880
|
C | T | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.79+1473C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595880 | ||||||
chr6:87595889
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.79+1482G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595889 | ||||||
chr6:87595921
|
A | C | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.79+1514A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595921 | ||||||
chr6:87595924
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.79+1517C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595924 | ||||||
chr6:87595924
|
C | T | 2 | a0002c0003t0003g0350a0002c0003t0003g0351 | 2 | HG01433.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.79+1517C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595924 | ||||||
chr6:87595987
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.79+1580T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595987 | ||||||
chr6:87595992
|
C | T | 3 | a0003c0004t0001g0229a0003c0004t0001g0230a0003c0004t0006g0231 | 3 | HG02258.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.79+1585C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87595992 | ||||||
chr6:87596079
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79+1672G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87596079 | ||||||
chr6:87596160
|
G | GT | 31 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0282others(28): Show | 32 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.79+1765dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87596160 | |||||
chr6:87596177
|
C | A | 117 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(114): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.79+1770C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87596177 | ||||||
chr6:87596177
|
C | T | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 60 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.79+1770C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87596177 | ||||||
chr6:87596448
|
G | GT | 187 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(184): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.79+2054dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87596448 | |||||
chr6:87596450
|
T | TG | 4 | a0001c0001t0001g0149a0001c0002t0001g0340a0001c0002t0001g0341others(1): Show | 4 | HG02109.hp2 NA19043.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+2043_79+2044ins others(1): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87596450 | ||||||
chr6:87596597
|
A | C | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.79+2190A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87596597 | ||||||
chr6:87597162
|
A | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0104others(5): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+2755A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597162 | ||||||
chr6:87597355
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.79+2948G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597355 | ||||||
chr6:87597382
|
A | T | 10 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 10 | HG02056.hp2 HG02132.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+2975A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597382 | ||||||
chr6:87597416
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0104others(5): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+3009C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597416 | ||||||
chr6:87597554
|
A | G | 1 | a0002c0003t0003g0351 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.79+3147A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597554 | ||||||
chr6:87597660
|
T | A | 1 | a0001c0001t0001g0335 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.79+3253T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597660 | ||||||
chr6:87597668
|
GAT | G | 5 | a0001c0001t0001g0027a0002c0003t0003g0343a0003c0004t0001g0229others(2): Show | 5 | HG02145.hp1 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+3273_79+3274del others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597668 | |||||
chr6:87597668
|
GATAT | G | 8 | a0002c0003t0003g0344a0002c0003t0003g0345a0002c0003t0003g0346others(5): Show | 8 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+3271_79+3274del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597668 | |||||
chr6:87597678
|
TATAC | T | 4 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0335others(1): Show | 4 | HG02622.hp2 HG03927.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+3273_79+3276del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597678 | |||||
chr6:87597678
|
TATACAC | T | 5 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+3273_79+3278del others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597678 | |||||
chr6:87597678
|
TATACACA others(1): Show |
T | 13 | a0001c0001t0002g0013a0001c0001t0002g0287a0001c0001t0002g0288others(10): Show | 14 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.79+3273_79+3280del others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597678 | |||||
chr6:87597680
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 16 | HG00423.hp1 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+3273T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597680 | ||||||
chr6:87597680
|
T | TAC | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(26): Show | 29 | HG00741.hp1 HG01069.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+3303_79+3304dup others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597680 | |||||
chr6:87597680
|
T | TACAC | 7 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG01081.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+3301_79+3304dup others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597680 | |||||
chr6:87597680
|
TAC | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG02040.hp1 HG02486.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+3303_79+3304del others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597680 | |||||
chr6:87597680
|
TACAC | T | 77 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(74): Show | 81 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.79+3301_79+3304del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597680 | |||||
chr6:87597680
|
TACACAC | T | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+3299_79+3304del others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597680 | |||||
chr6:87597680
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79+3289_79+3304del others(16): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597680 | |||||
chr6:87597682
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.79+3275C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597682 | ||||||
chr6:87597708
|
CACAT | C | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302 | 3 | HG02809.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.79+3303_79+3306del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597708 | |||||
chr6:87597710
|
C | CACATAT | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+3304_79+3305ins others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87597710 | |||||
chr6:87597731
|
T | A | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG00741.hp1 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+3324T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597731 | ||||||
chr6:87597732
|
A | T | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+3325A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597732 | ||||||
chr6:87597754
|
A | C | 2 | a0001c0002t0001g0285a0001c0002t0001g0286 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.79+3347A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87597754 | ||||||
chr6:87598129
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0338a0001c0001t0001g0339 | 4 | HG01168.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-3655C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598129 | ||||||
chr6:87598287
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.80-3497C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598287 | ||||||
chr6:87598288
|
G | T | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.80-3496G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598288 | ||||||
chr6:87598395
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.80-3389A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598395 | ||||||
chr6:87598519
|
A | G | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-3265A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598519 | ||||||
chr6:87598569
|
C | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | NA18949.hp2 NA18966.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.80-3215C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598569 | ||||||
chr6:87598601
|
A | G | 11 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0162others(8): Show | 11 | HG00741.hp1 HG01358.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-3183A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598601 | ||||||
chr6:87598621
|
T | C | 1 | a0001c0002t0001g0293 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.80-3163T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598621 | ||||||
chr6:87598647
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.80-3137A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598647 | ||||||
chr6:87598658
|
C | CT | 7 | a0001c0001t0001g0226a0001c0001t0001g0232a0001c0001t0001g0257others(4): Show | 7 | HG01934.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-3112dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87598658 | |||||
chr6:87598893
|
C | T | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-2891C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598893 | ||||||
chr6:87598894
|
G | A | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.80-2890G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598894 | ||||||
chr6:87598909
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-2875A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87598909 | ||||||
chr6:87599018
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-2766C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599018 | ||||||
chr6:87599093
|
C | T | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.80-2691C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599093 | ||||||
chr6:87599158
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.80-2626A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599158 | ||||||
chr6:87599345
|
C | CT | 4 | a0001c0001t0001g0005a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 6 | HG03209.hp1 NA18950.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2431dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87599345 | |||||
chr6:87599353
|
T | A | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.80-2431T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599353 | ||||||
chr6:87599353
|
T | TTATTA | 26 | a0001c0001t0001g0237a0001c0001t0001g0243a0001c0001t0001g0244others(23): Show | 26 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.80-2431_80-2430ins others(5): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599353 | ||||||
chr6:87599354
|
A | ATTAT | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.80-2403_80-2400dup others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87599354 | |||||
chr6:87599354
|
A | ATTATTTA others(1): Show |
28 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0162others(25): Show | 29 | HG00741.hp1 HG01358.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.80-2407_80-2400dup others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87599354 | |||||
chr6:87599354
|
A | ATTATTTA others(5): Show |
11 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0342others(8): Show | 11 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-2411_80-2400dup others(12): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87599354 | |||||
chr6:87599354
|
A | ATTATTTA others(9): Show |
4 | a0001c0002t0001g0340a0001c0002t0001g0341a0002c0003t0003g0344others(1): Show | 4 | NA18947.hp2 NA19043.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-2415_80-2400dup others(16): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87599354 | |||||
chr6:87599354
|
A | T | 27 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0243others(24): Show | 27 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.80-2430A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599354 | ||||||
chr6:87599354
|
ATTAT | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-2403_80-2400del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87599354 | |||||
chr6:87599482
|
C | T | 165 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.80-2302C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599482 | ||||||
chr6:87599524
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.80-2260C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599524 | ||||||
chr6:87599529
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80-2255G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599529 | ||||||
chr6:87599609
|
G | A | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-2175G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599609 | ||||||
chr6:87599755
|
C | G | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-2029C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599755 | ||||||
chr6:87599804
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | NA18967.hp1 NA19058.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1980C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599804 | ||||||
chr6:87599822
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.80-1962A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599822 | ||||||
chr6:87599845
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.80-1939C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599845 | ||||||
chr6:87599865
|
C | T | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.80-1919C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599865 | ||||||
chr6:87599866
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.80-1918G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599866 | ||||||
chr6:87599987
|
G | A | 247 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(244): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.80-1797G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87599987 | ||||||
chr6:87600265
|
C | T | 7 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG01081.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-1519C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87600265 | ||||||
chr6:87600609
|
G | A | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-1175G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87600609 | ||||||
chr6:87600754
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.80-1030A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87600754 | ||||||
chr6:87600803
|
G | GTATT | 247 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(244): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.80-978_80-977insTT others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 87600803 | |||||
chr6:87600905
|
A | G | 247 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(244): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.80-879A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87600905 | ||||||
chr6:87600913
|
T | C | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.80-871T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87600913 | ||||||
chr6:87600968
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.80-816T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87600968 | ||||||
chr6:87601118
|
G | A | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-666G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601118 | ||||||
chr6:87601174
|
A | C | 1 | a0003c0004t0006g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.80-610A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601174 | ||||||
chr6:87601184
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.80-600G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601184 | ||||||
chr6:87601542
|
T | C | 248 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(245): Show | 255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.80-242T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601542 | ||||||
chr6:87601543
|
G | A | 165 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.80-241G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601543 | ||||||
chr6:87601610
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02723.hp2 HG03098.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.80-174C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601610 | ||||||
chr6:87601688
|
T | C | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-96T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601688 | ||||||
chr6:87601739
|
C | A | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-45C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 2/19 | chr6 | 87601739 | ||||||
chr6:87602193
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0018others(6): Show | 12 | HG00423.hp2 HG02135.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.177+312C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602193 | ||||||
chr6:87602257
|
A | G | 166 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.177+376A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602257 | ||||||
chr6:87602271
|
G | A | 1 | a0001c0001t0004g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.177+390G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602271 | ||||||
chr6:87602275
|
A | G | 50 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 54 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.177+394A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602275 | ||||||
chr6:87602428
|
C | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | HG02615.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.177+547C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602428 | ||||||
chr6:87602462
|
GA | G | 6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 6 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+582delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602462 | ||||||
chr6:87602467
|
C | CT | 11 | a0001c0001t0001g0086a0001c0001t0001g0227a0002c0003t0003g0343others(8): Show | 11 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+601dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602467 | |||||
chr6:87602605
|
A | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG00544.hp2 HG02129.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+724A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602605 | ||||||
chr6:87602720
|
T | C | 2 | a0001c0001t0001g0086a0001c0008t0001g0039 | 2 | HG02698.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.178-664T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602720 | ||||||
chr6:87602891
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-493A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602891 | ||||||
chr6:87602905
|
T | TTA | 12 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0040others(9): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-473_178-472dup others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602905 | |||||
chr6:87602905
|
TTATATAT others(2): Show |
T | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.178-471_178-463del others(9): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602905 | |||||
chr6:87602911
|
AT | A | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.178-471delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602911 | |||||
chr6:87602912
|
T | TATTATAT others(1): Show |
48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.178-472_178-471ins others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602912 | ||||||
chr6:87602912
|
T | TATTATAT others(10): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.178-472_178-471ins others(17): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602912 | ||||||
chr6:87602913
|
T | A | 48 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(45): Show | 48 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.178-471T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602913 | ||||||
chr6:87602914
|
A | AT | 50 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 54 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.178-469dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602914 | |||||
chr6:87602914
|
A | T | 48 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(45): Show | 48 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.178-470A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602914 | ||||||
chr6:87602915
|
TA | T | 27 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.178-468delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602915 | ||||||
chr6:87602925
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.178-459T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602925 | ||||||
chr6:87602934
|
A | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0104others(5): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-450A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602934 | ||||||
chr6:87602952
|
A | ATT | 5 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-431_178-430ins others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602952 | |||||
chr6:87602953
|
T | TTTTA | 3 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0294 | 3 | HG02257.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.178-431_178-430ins others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602953
|
T | TTTTATTT others(11): Show |
1 | a0002c0003t0003g0347 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.178-431_178-430ins others(18): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602953
|
T | TTTTATTT others(17): Show |
1 | a0002c0003t0003g0348 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.178-431_178-430ins others(24): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602953
|
T | TTTTATTT others(21): Show |
3 | a0002c0003t0003g0344a0002c0003t0003g0346a0002c0003t0003g0349 | 3 | HG01256.hp2 NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.178-431_178-430ins others(28): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602953
|
T | TTTTATTT others(23): Show |
2 | a0002c0003t0003g0343a0002c0003t0003g0350 | 2 | HG02145.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.178-431_178-430ins others(30): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602953
|
T | TTTTATTT others(25): Show |
2 | a0002c0003t0003g0345a0002c0003t0003g0351 | 2 | HG01433.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.178-431_178-430ins others(32): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602953
|
TAATA | T | 4 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342others(1): Show | 4 | HG02109.hp2 HG02486.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-430_178-427del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602953 | ||||||
chr6:87602954
|
A | AATACATA others(13): Show |
1 | a0001c0001t0001g0253 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.178-427_178-426ins others(20): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0279a0001c0001t0004g0239a0001c0001t0004g0240 | 3 | HG03041.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.178-422_178-413dup others(10): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(5): Show |
3 | a0001c0001t0001g0252a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG01167.hp1 NA18968.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.178-424_178-413dup others(12): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(7): Show |
5 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0268others(2): Show | 5 | HG01346.hp1 HG02896.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-426_178-413dup others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(9): Show |
7 | a0001c0001t0001g0241a0001c0001t0001g0249a0001c0001t0001g0254others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-428_178-413dup others(16): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(11): Show |
16 | a0001c0001t0001g0014a0001c0001t0001g0234a0001c0001t0001g0260others(13): Show | 17 | HG00733.hp2 HG01934.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-413_178-412ins others(18): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(13): Show |
22 | a0001c0001t0001g0015a0001c0001t0001g0242a0001c0001t0001g0255others(19): Show | 23 | HG01074.hp1 HG01123.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-413_178-412ins others(20): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(15): Show |
5 | a0001c0001t0001g0251a0001c0001t0001g0265a0001c0001t0001g0302others(2): Show | 5 | HG02523.hp1 NA18957.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-413_178-412ins others(22): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(17): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 9 | HG00741.hp2 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.178-413_178-412ins others(24): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(19): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0237a0001c0001t0001g0270others(4): Show | 8 | HG01106.hp1 HG01516.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-413_178-412ins others(26): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(32): Show |
1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.178-413_178-412ins others(39): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(21): Show |
4 | a0001c0001t0001g0266a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG00735.hp1 HG00735.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-413_178-412ins others(28): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(27): Show |
1 | a0001c0001t0001g0333 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.178-413_178-412ins others(34): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(33): Show |
1 | a0001c0001t0001g0267 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.178-413_178-412ins others(40): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | AATATATA others(18): Show |
1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-413_178-412ins others(25): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602954 | |||||
chr6:87602954
|
A | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(20): Show | 24 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.178-430A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602954 | ||||||
chr6:87602955
|
A | T | 6 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(3): Show | 7 | HG02145.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-429A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602955 | ||||||
chr6:87602958
|
TATATATA others(7): Show |
T | 124 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(121): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.178-414_178-401del others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602958 | |||||
chr6:87602959
|
A | T | 4 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342others(1): Show | 4 | HG02109.hp2 HG02486.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-425A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602959 | ||||||
chr6:87602960
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.178-410_178-399del others(12): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602960 | |||||
chr6:87602962
|
T | TATATATA others(31): Show |
1 | a0001c0001t0001g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.178-413_178-412ins others(38): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602962 | |||||
chr6:87602968
|
TATAC | T | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG04204.hp1 NA18971.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-412_178-409del others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 87602968 | |||||
chr6:87602972
|
C | T | 117 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(114): Show | 122 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.178-412C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602972 | ||||||
chr6:87602982
|
T | C | 2 | a0003c0004t0001g0229a0003c0004t0001g0230 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.178-402T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87602982 | ||||||
chr6:87603081
|
G | A | 18 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0013others(15): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-303G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87603081 | ||||||
chr6:87603170
|
A | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.178-214A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 3/19 | chr6 | 87603170 | ||||||
chr6:87603655
|
T | C | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.322+127T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87603655 | ||||||
chr6:87603879
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.322+351G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87603879 | ||||||
chr6:87603987
|
T | C | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.322+459T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87603987 | ||||||
chr6:87604190
|
G | C | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.322+662G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87604190 | ||||||
chr6:87604374
|
G | C | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.322+846G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87604374 | ||||||
chr6:87604412
|
A | G | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.322+884A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87604412 | ||||||
chr6:87604615
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.322+1087A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87604615 | ||||||
chr6:87604846
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.323-1071C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87604846 | ||||||
chr6:87605025
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.323-892G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605025 | ||||||
chr6:87605095
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.323-822C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605095 | ||||||
chr6:87605140
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.323-777C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605140 | ||||||
chr6:87605636
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.323-281C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605636 | ||||||
chr6:87605649
|
C | CA | 9 | a0001c0001t0001g0042a0001c0001t0001g0179a0001c0001t0001g0225others(6): Show | 9 | HG02886.hp2 HG03486.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.323-254dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 87605649 | |||||
chr6:87605665
|
A | C | 1 | a0001c0001t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.323-252A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605665 | ||||||
chr6:87605845
|
T | C | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.323-72T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605845 | ||||||
chr6:87605885
|
T | C | 1 | a0001c0001t0004g0239 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.323-32T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605885 | ||||||
chr6:87605914
|
T | A | 1 | a0001c0001t0001g0243 | 1 | NA19079.hp1 | splice_region_variant&intron_variant | LOW | c.323-3T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 4/19 | chr6 | 87605914 | ||||||
chr6:87606023
|
TA | T | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
splice_region_variant&intron_variant | LOW | c.427+7delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 87606023 | |||||
chr6:87606036
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | NA18949.hp2 NA18966.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.427+15G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87606036 | ||||||
chr6:87606077
|
CT | C | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.427+60delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 87606077 | |||||
chr6:87606133
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.427+112G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87606133 | ||||||
chr6:87606468
|
G | C | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.427+447G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87606468 | ||||||
chr6:87606530
|
CT | C | 24 | a0001c0001t0001g0273a0001c0001t0001g0282a0001c0001t0001g0283others(21): Show | 24 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.427+522delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 87606530 | |||||
chr6:87606553
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.427+532C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87606553 | ||||||
chr6:87606687
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.427+666G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87606687 | ||||||
chr6:87606779
|
C | A | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+758C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87606779 | ||||||
chr6:87607012
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-661G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607012 | ||||||
chr6:87607014
|
C | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-659C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607014 | ||||||
chr6:87607015
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-658A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607015 | ||||||
chr6:87607019
|
G | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-654G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607019 | ||||||
chr6:87607030
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-643G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607030 | ||||||
chr6:87607032
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-641G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607032 | ||||||
chr6:87607033
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-640A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607033 | ||||||
chr6:87607034
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-639A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607034 | ||||||
chr6:87607038
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-635G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607038 | ||||||
chr6:87607041
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-632A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607041 | ||||||
chr6:87607045
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-628G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607045 | ||||||
chr6:87607050
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-623T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607050 | ||||||
chr6:87607066
|
A | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-607A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607066 | ||||||
chr6:87607073
|
T | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-600T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607073 | ||||||
chr6:87607074
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-599A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607074 | ||||||
chr6:87607076
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-597T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607076 | ||||||
chr6:87607077
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-596C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607077 | ||||||
chr6:87607078
|
C | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-595C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607078 | ||||||
chr6:87607080
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-593A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607080 | ||||||
chr6:87607083
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-590A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607083 | ||||||
chr6:87607084
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-589T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607084 | ||||||
chr6:87607086
|
T | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-587T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607086 | ||||||
chr6:87607088
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-585T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607088 | ||||||
chr6:87607094
|
G | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-579G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607094 | ||||||
chr6:87607095
|
C | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-578C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607095 | ||||||
chr6:87607101
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-572T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607101 | ||||||
chr6:87607108
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-565T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607108 | ||||||
chr6:87607109
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-564T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607109 | ||||||
chr6:87607110
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-563G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607110 | ||||||
chr6:87607111
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-562C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607111 | ||||||
chr6:87607112
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-561T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607112 | ||||||
chr6:87607116
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-557G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607116 | ||||||
chr6:87607118
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-555G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607118 | ||||||
chr6:87607120
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-553C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607120 | ||||||
chr6:87607122
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-551T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607122 | ||||||
chr6:87607123
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-550T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607123 | ||||||
chr6:87607125
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-548T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607125 | ||||||
chr6:87607128
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-545T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607128 | ||||||
chr6:87607131
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-542T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607131 | ||||||
chr6:87607133
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-540G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607133 | ||||||
chr6:87607135
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-538T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607135 | ||||||
chr6:87607139
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-534A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607139 | ||||||
chr6:87607146
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-527A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607146 | ||||||
chr6:87607148
|
T | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-525T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607148 | ||||||
chr6:87607152
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-521T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607152 | ||||||
chr6:87607155
|
G | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-518G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607155 | ||||||
chr6:87607158
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-515C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607158 | ||||||
chr6:87607159
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-514A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607159 | ||||||
chr6:87607163
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-510T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607163 | ||||||
chr6:87607164
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-509T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607164 | ||||||
chr6:87607166
|
G | C | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-507G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607166 | ||||||
chr6:87607170
|
C | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-503C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607170 | ||||||
chr6:87607171
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.428-502T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607171 | ||||||
chr6:87607226
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.428-447C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607226 | ||||||
chr6:87607557
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.428-116A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607557 | ||||||
chr6:87607570
|
C | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.428-103C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | chr6 | 87607570 | ||||||
chr6:87607574
|
CA | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.428-89delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 87607574 | |||||
chr6:87607852
|
A | G | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.579+28A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87607852 | ||||||
chr6:87607865
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.579+41A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87607865 | ||||||
chr6:87607883
|
A | C | 1 | a0001c0001t0001g0302 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.579+59A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87607883 | ||||||
chr6:87607900
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.579+76C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87607900 | ||||||
chr6:87607910
|
C | G | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.579+86C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87607910 | ||||||
chr6:87607957
|
G | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.579+133G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87607957 | ||||||
chr6:87608330
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.579+506A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608330 | ||||||
chr6:87608489
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.580-607A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608489 | ||||||
chr6:87608530
|
T | G | 40 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(37): Show | 40 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.580-566T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608530 | ||||||
chr6:87608659
|
A | T | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.580-437A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608659 | ||||||
chr6:87608676
|
T | C | 4 | a0003c0004t0001g0146a0003c0004t0001g0229a0003c0004t0001g0230others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-420T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608676 | ||||||
chr6:87608729
|
A | AT | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.580-360dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 87608729 | |||||
chr6:87608756
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.580-340C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608756 | ||||||
chr6:87608828
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.580-268T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608828 | ||||||
chr6:87608830
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.580-266T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608830 | ||||||
chr6:87608872
|
T | TAAA | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-223_580-222ins others(3): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 87608872 | |||||
chr6:87608874
|
T | A | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-222T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608874 | ||||||
chr6:87608875
|
G | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-221G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608875 | ||||||
chr6:87608877
|
G | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-219G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608877 | ||||||
chr6:87608879
|
T | C | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-217T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608879 | ||||||
chr6:87608881
|
T | A | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-215T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608881 | ||||||
chr6:87608996
|
T | C | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.580-100T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 6/19 | chr6 | 87608996 | ||||||
chr6:87609519
|
G | A | 4 | a0001c0001t0001g0309a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02056.hp1 NA19057.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.713+290G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87609519 | ||||||
chr6:87609618
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.713+389G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87609618 | ||||||
chr6:87609713
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.713+484G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87609713 | ||||||
chr6:87609783
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.713+554C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87609783 | ||||||
chr6:87610165
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.713+936C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610165 | ||||||
chr6:87610201
|
AT | A | 3 | a0001c0005t0002g0276a0001c0005t0002g0277a0001c0005t0002g0278 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.713+973delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610201 | ||||||
chr6:87610524
|
TTACTAAT others(321): Show |
T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.713+1311_714-1222d others(2): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 87610524 | |||||
chr6:87610556
|
A | T | 55 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(52): Show | 59 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.713+1327A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610556 | ||||||
chr6:87610557
|
T | A | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.713+1328T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610557 | ||||||
chr6:87610558
|
T | A | 2 | a0001c0001t0001g0328a0001c0001t0001g0330 | 2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.713+1329T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610558 | ||||||
chr6:87610647
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.713+1418G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610647 | ||||||
chr6:87610699
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.714-1390G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610699 | ||||||
chr6:87610805
|
G | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.714-1284G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610805 | ||||||
chr6:87610808
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.714-1281C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610808 | ||||||
chr6:87610848
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.714-1241C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610848 | ||||||
chr6:87610923
|
T | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.714-1166T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610923 | ||||||
chr6:87610934
|
C | CT | 166 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0079others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.714-1135dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 87610934 | |||||
chr6:87610934
|
C | CTT | 7 | a0001c0001t0001g0148a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG02257.hp1 HG02683.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.714-1136_714-1135d others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 87610934 | |||||
chr6:87610977
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.714-1112C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87610977 | ||||||
chr6:87611027
|
C | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.714-1062C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611027 | ||||||
chr6:87611033
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.714-1056C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611033 | ||||||
chr6:87611080
|
G | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.714-1009G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611080 | ||||||
chr6:87611162
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.714-927C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611162 | ||||||
chr6:87611164
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0098 | 3 | HG01081.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.714-925T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611164 | ||||||
chr6:87611172
|
A | G | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 8 | HG01099.hp2 HG02300.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.714-917A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611172 | ||||||
chr6:87611324
|
G | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(51): Show | 58 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.714-765G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611324 | ||||||
chr6:87611459
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.714-630A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611459 | ||||||
chr6:87611503
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.714-586C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611503 | ||||||
chr6:87611652
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0180 | 2 | HG01069.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.714-437C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611652 | ||||||
chr6:87611730
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19003.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.714-359C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611730 | ||||||
chr6:87611865
|
T | C | 4 | a0001c0002t0001g0285a0001c0002t0001g0286a0001c0002t0001g0293others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-224T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611865 | ||||||
chr6:87611923
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.714-166T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87611923 | ||||||
chr6:87612037
|
G | A | 6 | a0001c0001t0001g0307a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.714-52G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 7/19 | chr6 | 87612037 | ||||||
chr6:87612279
|
G | A | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 55 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.873+31G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87612279 | ||||||
chr6:87612328
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0027 | 3 | NA18963.hp2 NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.873+80A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87612328 | ||||||
chr6:87612556
|
A | T | 1 | a0001c0001t0001g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.873+308A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87612556 | ||||||
chr6:87612873
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.873+625G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87612873 | ||||||
chr6:87612914
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.873+666C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87612914 | ||||||
chr6:87612974
|
A | G | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.873+726A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87612974 | ||||||
chr6:87613273
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.873+1025C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87613273 | ||||||
chr6:87613420
|
A | G | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.873+1172A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87613420 | ||||||
chr6:87613513
|
C | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.873+1265C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87613513 | ||||||
chr6:87613726
|
C | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.873+1478C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87613726 | ||||||
chr6:87613729
|
C | T | 1 | a0003c0004t0006g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.873+1481C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87613729 | ||||||
chr6:87613806
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.873+1558G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87613806 | ||||||
chr6:87614139
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.873+1891T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614139 | ||||||
chr6:87614160
|
C | T | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.873+1912C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614160 | ||||||
chr6:87614237
|
C | G | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.873+1989C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614237 | ||||||
chr6:87614295
|
T | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(51): Show | 58 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.874-2019T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614295 | ||||||
chr6:87614359
|
G | T | 4 | a0003c0004t0001g0146a0003c0004t0001g0229a0003c0004t0001g0230others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-1955G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614359 | ||||||
chr6:87614424
|
T | C | 252 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(249): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.874-1890T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614424 | ||||||
chr6:87614553
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.874-1761T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614553 | ||||||
chr6:87614617
|
T | C | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.874-1697T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614617 | ||||||
chr6:87614861
|
A | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.874-1453A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87614861 | ||||||
chr6:87615033
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.874-1281A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615033 | ||||||
chr6:87615116
|
G | C | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.874-1198G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615116 | ||||||
chr6:87615202
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.874-1112A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615202 | ||||||
chr6:87615326
|
G | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.874-988G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615326 | ||||||
chr6:87615552
|
G | A | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 55 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.874-762G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615552 | ||||||
chr6:87615778
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.874-536G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615778 | ||||||
chr6:87615924
|
C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.874-390C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615924 | ||||||
chr6:87615942
|
G | T | 1 | a0001c0001t0001g0318 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.874-372G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615942 | ||||||
chr6:87615944
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.874-370A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | chr6 | 87615944 | ||||||
chr6:87616016
|
G | GA | 38 | a0001c0001t0001g0037a0001c0001t0001g0234a0001c0001t0001g0235others(35): Show | 38 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.874-288dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr6 | 87616016 | |||||
chr6:87616547
|
C | T | 2 | a0001c0001t0001g0306a0001c0001t0001g0333 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.987+120C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87616547 | ||||||
chr6:87616684
|
A | G | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.987+257A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87616684 | ||||||
chr6:87616859
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.987+432G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87616859 | ||||||
chr6:87616883
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.987+456C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87616883 | ||||||
chr6:87617053
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.987+626T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617053 | ||||||
chr6:87617136
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.987+709G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617136 | ||||||
chr6:87617207
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.987+780A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617207 | ||||||
chr6:87617470
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.987+1043C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617470 | ||||||
chr6:87617598
|
G | A | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.987+1171G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617598 | ||||||
chr6:87617620
|
G | C | 217 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(214): Show | 223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.987+1193G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617620 | ||||||
chr6:87617637
|
G | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.987+1210G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617637 | ||||||
chr6:87617782
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.987+1355A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617782 | ||||||
chr6:87617861
|
G | T | 1 | a0001c0002t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.987+1434G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87617861 | ||||||
chr6:87617948
|
T | TAAAAGAA others(311): Show |
1 | a0001c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.987+1535_987+1536i others(320): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 87617948 | |||||
chr6:87618028
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.987+1601A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618028 | ||||||
chr6:87618176
|
C | T | 6 | a0001c0001t0001g0307a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+1749C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618176 | ||||||
chr6:87618279
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0137a0001c0001t0001g0233 | 3 | NA18971.hp1 NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.987+1852G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618279 | ||||||
chr6:87618301
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.987+1874T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618301 | ||||||
chr6:87618356
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.987+1929C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618356 | ||||||
chr6:87618411
|
C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.987+1984C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618411 | ||||||
chr6:87618416
|
C | CAA | 211 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(208): Show | 217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.987+2001_987+2002d others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 87618416 | |||||
chr6:87618416
|
C | CAAA | 25 | a0001c0001t0001g0123a0001c0001t0001g0184a0001c0001t0001g0253others(22): Show | 25 | HG00323.hp1 HG01243.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.987+2000_987+2002d others(5): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 87618416 | |||||
chr6:87618515
|
G | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.987+2088G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618515 | ||||||
chr6:87618535
|
A | G | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.987+2108A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618535 | ||||||
chr6:87618549
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.987+2122G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618549 | ||||||
chr6:87618635
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0171a0001c0001t0001g0172others(2): Show | 5 | HG02559.hp1 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+2208T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618635 | ||||||
chr6:87618704
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.987+2277A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87618704 | ||||||
chr6:87619010
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.988-2344A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619010 | ||||||
chr6:87619318
|
A | G | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.988-2036A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619318 | ||||||
chr6:87619438
|
G | A | 3 | a0002c0003t0003g0344a0002c0003t0003g0345a0002c0003t0003g0346 | 3 | NA18947.hp2 NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.988-1916G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619438 | ||||||
chr6:87619448
|
C | T | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302 | 3 | HG02809.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.988-1906C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619448 | ||||||
chr6:87619641
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.988-1713G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619641 | ||||||
chr6:87619709
|
A | G | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.988-1645A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619709 | ||||||
chr6:87619792
|
C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.988-1562C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619792 | ||||||
chr6:87619910
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0098 | 3 | HG01081.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.988-1444G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87619910 | ||||||
chr6:87620224
|
C | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.988-1130C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87620224 | ||||||
chr6:87620324
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.988-1030C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87620324 | ||||||
chr6:87620453
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.988-901A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87620453 | ||||||
chr6:87620733
|
G | A | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.988-621G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87620733 | ||||||
chr6:87620884
|
T | A | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.988-470T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87620884 | ||||||
chr6:87621153
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0224 | 2 | HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.988-201C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87621153 | ||||||
chr6:87621180
|
G | GA | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.988-174_988-173ins others(1): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87621180 | ||||||
chr6:87621246
|
A | G | 5 | a0002c0003t0003g0347a0002c0003t0003g0348a0002c0003t0003g0349others(2): Show | 5 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-108A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87621246 | ||||||
chr6:87621340
|
C | T | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.988-14C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 9/19 | chr6 | 87621340 | ||||||
chr6:87621581
|
A | G | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1121+94A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 10/19 | chr6 | 87621581 | ||||||
chr6:87621616
|
TC | T | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1121+132delC | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 87621616 | |||||
chr6:87621710
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1121+223A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 10/19 | chr6 | 87621710 | ||||||
chr6:87621929
|
A | G | 3 | a0001c0005t0002g0276a0001c0005t0002g0277a0001c0005t0002g0278 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1122-21A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 10/19 | chr6 | 87621929 | ||||||
chr6:87622103
|
A | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0304others(14): Show | 19 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1185+90A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622103 | ||||||
chr6:87622125
|
A | G | 3 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0317 | 3 | HG02895.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1185+112A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622125 | ||||||
chr6:87622212
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1185+199T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622212 | ||||||
chr6:87622405
|
T | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1185+392T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622405 | ||||||
chr6:87622421
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1185+408T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622421 | ||||||
chr6:87622444
|
T | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1185+431T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622444 | ||||||
chr6:87622594
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1185+581T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622594 | ||||||
chr6:87622623
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1185+610T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622623 | ||||||
chr6:87622640
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1185+627C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622640 | ||||||
chr6:87622647
|
C | CCT | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+635_1185+636d others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87622647 | |||||
chr6:87622858
|
A | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1185+845A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622858 | ||||||
chr6:87622964
|
A | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1185+951A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87622964 | ||||||
chr6:87623045
|
G | A | 1 | a0009c0013t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1185+1032G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623045 | ||||||
chr6:87623256
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0077 | 2 | NA18940.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1185+1243C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623256 | ||||||
chr6:87623422
|
G | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+1409G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623422 | ||||||
chr6:87623489
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1185+1476T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623489 | ||||||
chr6:87623513
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1185+1500G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623513 | ||||||
chr6:87623534
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0054others(11): Show | 17 | HG00408.hp2 HG00733.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1185+1521C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623534 | ||||||
chr6:87623611
|
C | T | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1185+1598C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623611 | ||||||
chr6:87623644
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1185+1631G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623644 | ||||||
chr6:87623799
|
A | G | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1185+1786A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623799 | ||||||
chr6:87623832
|
C | T | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1185+1819C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623832 | ||||||
chr6:87623859
|
G | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+1846G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87623859 | ||||||
chr6:87623884
|
TA | T | 24 | a0001c0001t0001g0123a0001c0001t0001g0282a0001c0001t0001g0283others(21): Show | 24 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.1185+1880delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87623884 | |||||
chr6:87624176
|
G | A | 118 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1185+2163G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624176 | ||||||
chr6:87624213
|
G | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG02056.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1185+2200G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624213 | ||||||
chr6:87624258
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1185+2245C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624258 | ||||||
chr6:87624292
|
T | G | 3 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355 | 3 | HG00597.hp1 NA19003.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1185+2279T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624292 | ||||||
chr6:87624451
|
C | G | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+2438C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624451 | ||||||
chr6:87624452
|
G | A | 1 | a0001c0001t0001g0254 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1185+2439G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624452 | ||||||
chr6:87624475
|
C | A | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1185+2462C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624475 | ||||||
chr6:87624539
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1185+2526A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624539 | ||||||
chr6:87624578
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1185+2565A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624578 | ||||||
chr6:87624702
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1185+2689T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624702 | ||||||
chr6:87624766
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG01069.hp2 HG02055.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185+2753T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624766 | ||||||
chr6:87624846
|
AC | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+2838delC | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87624846 | |||||
chr6:87624882
|
C | T | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.1185+2869C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87624882 | ||||||
chr6:87625012
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1185+2999A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625012 | ||||||
chr6:87625093
|
T | C | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+3080T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625093 | ||||||
chr6:87625130
|
A | G | 2 | a0003c0004t0001g0229a0003c0004t0001g0230 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1185+3117A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625130 | ||||||
chr6:87625245
|
G | A | 1 | a0001c0008t0001g0039 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1185+3232G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625245 | ||||||
chr6:87625331
|
A | G | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1185+3318A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625331 | ||||||
chr6:87625414
|
T | G | 2 | a0001c0001t0001g0188a0008c0011t0001g0187 | 2 | NA19000.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1185+3401T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625414 | ||||||
chr6:87625448
|
G | C | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01109.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185+3435G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625448 | ||||||
chr6:87625450
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1185+3437T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625450 | ||||||
chr6:87625483
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1185+3470G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625483 | ||||||
chr6:87625525
|
C | T | 162 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(159): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1185+3512C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625525 | ||||||
chr6:87625717
|
T | C | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1185+3704T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625717 | ||||||
chr6:87625868
|
G | A | 1 | a0001c0002t0001g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1185+3855G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625868 | ||||||
chr6:87625929
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0082 | 4 | HG01069.hp1 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185+3916T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87625929 | ||||||
chr6:87626019
|
G | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1185+4006G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87626019 | ||||||
chr6:87626085
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1185+4072G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87626085 | ||||||
chr6:87626230
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1185+4217T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87626230 | ||||||
chr6:87626787
|
CA | C | 235 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(232): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1185+4790delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87626787 | |||||
chr6:87626970
|
C | T | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1185+4957C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87626970 | ||||||
chr6:87627062
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1185+5049A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627062 | ||||||
chr6:87627150
|
A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0295a0001c0001t0001g0299others(4): Show | 8 | HG00735.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185+5137A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627150 | ||||||
chr6:87627158
|
C | T | 1 | a0003c0004t0006g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1185+5145C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627158 | ||||||
chr6:87627171
|
G | T | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1185+5158G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627171 | ||||||
chr6:87627228
|
A | C | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1185+5215A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627228 | ||||||
chr6:87627256
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1185+5243C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627256 | ||||||
chr6:87627289
|
G | A | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1185+5276G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627289 | ||||||
chr6:87627297
|
C | CT | 40 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0077others(37): Show | 40 | HG00423.hp1 HG01109.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.1185+5302dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87627297 | |||||
chr6:87627297
|
C | CTTTTTT | 9 | a0001c0001t0001g0283a0001c0002t0001g0284a0001c0002t0001g0285others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1185+5297_1185+530 others(10): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87627297 | |||||
chr6:87627297
|
C | CTTTTTTT | 10 | a0001c0002t0001g0286a0001c0002t0001g0294a0001c0002t0001g0342others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185+5296_1185+530 others(11): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87627297 | |||||
chr6:87627297
|
CT | C | 11 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0149others(8): Show | 11 | HG01069.hp2 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1185+5302delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87627297 | |||||
chr6:87627331
|
T | C | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+5318T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627331 | ||||||
chr6:87627335
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1185+5322G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627335 | ||||||
chr6:87627404
|
T | G | 1 | a0002c0003t0003g0343 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1185+5391T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627404 | ||||||
chr6:87627646
|
TTATAA | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+5638_1185+564 others(9): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87627646 | |||||
chr6:87627862
|
G | A | 40 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(37): Show | 40 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1185+5849G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627862 | ||||||
chr6:87627905
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1185+5892G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87627905 | ||||||
chr6:87628209
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1185+6196A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628209 | ||||||
chr6:87628222
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1185+6209G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628222 | ||||||
chr6:87628305
|
C | G | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1185+6292C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628305 | ||||||
chr6:87628532
|
A | G | 3 | a0001c0005t0002g0276a0001c0005t0002g0277a0001c0005t0002g0278 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1186-6313A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628532 | ||||||
chr6:87628655
|
A | G | 162 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(159): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1186-6190A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628655 | ||||||
chr6:87628706
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG00544.hp2 HG02129.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186-6139C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628706 | ||||||
chr6:87628835
|
CAG | C | 3 | a0001c0001t0002g0108a0001c0002t0001g0293a0001c0002t0001g0294 | 3 | HG02257.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1186-6009_1186-600 others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628835 | ||||||
chr6:87628868
|
A | C | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1186-5977A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87628868 | ||||||
chr6:87629034
|
T | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1186-5811T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629034 | ||||||
chr6:87629082
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1186-5763A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629082 | ||||||
chr6:87629083
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG01070.hp2 HG01123.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186-5762A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629083 | ||||||
chr6:87629378
|
T | C | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1186-5467T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629378 | ||||||
chr6:87629462
|
T | C | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1186-5383T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629462 | ||||||
chr6:87629533
|
G | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1186-5312G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629533 | ||||||
chr6:87629598
|
A | AG | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1186-5246dupG | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87629598 | |||||
chr6:87629693
|
G | C | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1186-5152G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629693 | ||||||
chr6:87629941
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1186-4904A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87629941 | ||||||
chr6:87630178
|
C | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0227 | 2 | NA19078.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1186-4667C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87630178 | ||||||
chr6:87630320
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1186-4525G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87630320 | ||||||
chr6:87630340
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1186-4505G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87630340 | ||||||
chr6:87630607
|
A | G | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1186-4238A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87630607 | ||||||
chr6:87630850
|
G | A | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(97): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1186-3995G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87630850 | ||||||
chr6:87631043
|
A | AT | 29 | a0001c0001t0001g0041a0001c0001t0001g0075a0001c0001t0001g0076others(26): Show | 29 | HG00544.hp1 HG01433.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.1186-3784dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87631043 | |||||
chr6:87631071
|
G | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1186-3774G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631071 | ||||||
chr6:87631147
|
C | A | 2 | a0001c0002t0001g0285a0001c0002t0001g0286 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1186-3698C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631147 | ||||||
chr6:87631258
|
T | G | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1186-3587T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631258 | ||||||
chr6:87631326
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1186-3519G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631326 | ||||||
chr6:87631487
|
G | T | 1 | a0003c0004t0006g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1186-3358G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631487 | ||||||
chr6:87631502
|
T | A | 1 | a0002c0003t0003g0343 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1186-3343T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631502 | ||||||
chr6:87631569
|
G | T | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1186-3276G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631569 | ||||||
chr6:87631579
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1186-3266G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631579 | ||||||
chr6:87631619
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1186-3226A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631619 | ||||||
chr6:87631652
|
C | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1186-3193C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631652 | ||||||
chr6:87631912
|
C | T | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1186-2933C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87631912 | ||||||
chr6:87632149
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1186-2696G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87632149 | ||||||
chr6:87632394
|
C | CA | 118 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1186-2447dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87632394 | |||||
chr6:87632495
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1186-2350A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87632495 | ||||||
chr6:87632714
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1186-2131G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87632714 | ||||||
chr6:87633221
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1186-1624C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87633221 | ||||||
chr6:87633375
|
T | A | 1 | a0001c0001t0001g0027 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1186-1470T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87633375 | ||||||
chr6:87633526
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1186-1319G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87633526 | ||||||
chr6:87633559
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1186-1286T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87633559 | ||||||
chr6:87633600
|
T | C | 217 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(214): Show | 223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1186-1245T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87633600 | ||||||
chr6:87634024
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1186-821T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634024 | ||||||
chr6:87634084
|
T | G | 2 | a0001c0002t0001g0285a0001c0002t0001g0286 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1186-761T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634084 | ||||||
chr6:87634116
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1186-729G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634116 | ||||||
chr6:87634126
|
G | A | 162 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(159): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1186-719G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634126 | ||||||
chr6:87634238
|
C | CT | 6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 6 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1186-597dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87634238 | |||||
chr6:87634247
|
T | G | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 55 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1186-598T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634247 | ||||||
chr6:87634302
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0007g0032 | 3 | HG01517.hp2 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1186-543G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634302 | ||||||
chr6:87634313
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1186-532A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634313 | ||||||
chr6:87634317
|
C | T | 2 | a0002c0003t0003g0344a0002c0003t0003g0345 | 2 | NA18947.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1186-528C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634317 | ||||||
chr6:87634624
|
A | G | 1 | a0003c0004t0001g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1186-221A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | chr6 | 87634624 | ||||||
chr6:87634740
|
A | ATCT | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1186-103_1186-101d others(5): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr6 | 87634740 | |||||
chr6:87635044
|
C | G | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1302+83C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635044 | ||||||
chr6:87635330
|
A | G | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1302+369A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635330 | ||||||
chr6:87635475
|
G | A | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1302+514G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635475 | ||||||
chr6:87635475
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1302+514G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635475 | ||||||
chr6:87635681
|
C | T | 1 | a0002c0003t0003g0346 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1302+720C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635681 | ||||||
chr6:87635790
|
T | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1303-617T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635790 | ||||||
chr6:87635791
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1303-616A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87635791 | ||||||
chr6:87635947
|
A | AT | 56 | a0001c0001t0001g0211a0001c0001t0001g0226a0001c0001t0001g0234others(53): Show | 56 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.1303-445dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 87635947 | |||||
chr6:87635947
|
A | ATT | 7 | a0001c0001t0001g0236a0001c0001t0001g0255a0001c0001t0001g0261others(4): Show | 7 | HG02056.hp2 HG03579.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-446_1303-445d others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 87635947 | |||||
chr6:87635947
|
AT | A | 32 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0095others(29): Show | 34 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1303-445delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 87635947 | |||||
chr6:87636134
|
G | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0302 | 3 | HG02809.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1303-273G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87636134 | ||||||
chr6:87636157
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1303-250C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87636157 | ||||||
chr6:87636167
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | NA19057.hp2 NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1303-240C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87636167 | ||||||
chr6:87636224
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0295others(18): Show | 23 | HG00735.hp2 HG01106.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1303-183G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 12/19 | chr6 | 87636224 | ||||||
chr6:87636651
|
T | C | 40 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(37): Show | 40 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1382+165T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87636651 | ||||||
chr6:87636841
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0095a0001c0001t0001g0096 | 5 | NA18950.hp1 NA18980.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.1382+355T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87636841 | ||||||
chr6:87637145
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1382+659G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637145 | ||||||
chr6:87637375
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1382+889T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637375 | ||||||
chr6:87637389
|
A | G | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1382+903A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637389 | ||||||
chr6:87637565
|
T | C | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1382+1079T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637565 | ||||||
chr6:87637587
|
T | C | 1 | a0001c0002t0001g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1382+1101T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637587 | ||||||
chr6:87637606
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1382+1120T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637606 | ||||||
chr6:87637893
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1382+1407A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87637893 | ||||||
chr6:87638693
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG01069.hp2 HG02055.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1382+2207T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87638693 | ||||||
chr6:87638910
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1382+2424T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87638910 | ||||||
chr6:87638927
|
A | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1382+2441A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87638927 | ||||||
chr6:87638958
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0295a0001c0001t0001g0299others(8): Show | 12 | HG00735.hp2 HG01106.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1382+2472G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87638958 | ||||||
chr6:87639210
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1382+2724C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639210 | ||||||
chr6:87639278
|
T | G | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1382+2792T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639278 | ||||||
chr6:87639294
|
C | T | 4 | a0001c0001t0001g0234a0001c0001t0001g0257a0001c0001t0001g0269others(1): Show | 4 | HG01934.hp2 HG02738.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+2808C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639294 | ||||||
chr6:87639400
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1382+2914C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639400 | ||||||
chr6:87639430
|
G | C | 1 | a0001c0002t0001g0290 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1382+2944G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639430 | ||||||
chr6:87639478
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1382+2992C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639478 | ||||||
chr6:87639805
|
C | A | 1 | a0005c0012t0001g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1382+3319C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639805 | ||||||
chr6:87639825
|
C | CA | 44 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 46 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1382+3364dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87639825 | |||||
chr6:87639825
|
C | CAA | 36 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(33): Show | 39 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1382+3363_1382+336 others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87639825 | |||||
chr6:87639825
|
C | CAAA | 8 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0322others(5): Show | 8 | HG00741.hp2 HG01123.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1382+3362_1382+336 others(7): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87639825 | |||||
chr6:87639825
|
CA | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0223a0001c0001t0001g0251others(3): Show | 6 | HG01256.hp1 HG02523.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1382+3364delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87639825 | |||||
chr6:87639895
|
G | A | 1 | a0003c0004t0001g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1382+3409G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87639895 | ||||||
chr6:87640027
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1382+3541G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640027 | ||||||
chr6:87640069
|
G | A | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1382+3583G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640069 | ||||||
chr6:87640083
|
G | A | 3 | a0001c0002t0001g0290a0001c0002t0001g0291a0001c0002t0001g0292 | 3 | HG02895.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1382+3597G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640083 | ||||||
chr6:87640084
|
C | T | 3 | a0001c0002t0001g0290a0001c0002t0001g0291a0001c0002t0001g0292 | 3 | HG02895.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1382+3598C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640084 | ||||||
chr6:87640139
|
TCAGC | T | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1382+3659_1382+366 others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87640139 | |||||
chr6:87640503
|
C | T | 6 | a0001c0001t0001g0307a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1382+4017C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640503 | ||||||
chr6:87640851
|
A | G | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1382+4365A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640851 | ||||||
chr6:87640856
|
T | A | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1382+4370T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640856 | ||||||
chr6:87640905
|
C | T | 1 | a0001c0008t0001g0039 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1382+4419C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87640905 | ||||||
chr6:87641057
|
C | T | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1382+4571C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87641057 | ||||||
chr6:87641337
|
ACTTTTCT others(21): Show |
A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | NA19005.hp1 NA19010.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1382+4856_1382+488 others(32): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87641337 | |||||
chr6:87641360
|
G | A | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1382+4874G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87641360 | ||||||
chr6:87641981
|
C | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1382+5495C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87641981 | ||||||
chr6:87642023
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1382+5537C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642023 | ||||||
chr6:87642282
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1382+5796A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642282 | ||||||
chr6:87642299
|
T | A | 23 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0284others(20): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1382+5813T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642299 | ||||||
chr6:87642407
|
G | A | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1382+5921G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642407 | ||||||
chr6:87642624
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1382+6138C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642624 | ||||||
chr6:87642640
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1382+6154C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642640 | ||||||
chr6:87642641
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1382+6155G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642641 | ||||||
chr6:87642758
|
C | G | 4 | a0001c0002t0001g0285a0001c0002t0001g0286a0001c0002t0001g0293others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+6272C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642758 | ||||||
chr6:87642794
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1382+6308C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642794 | ||||||
chr6:87642856
|
C | T | 3 | a0001c0005t0002g0276a0001c0005t0002g0277a0001c0005t0002g0278 | 3 | HG02615.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1382+6370C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642856 | ||||||
chr6:87642908
|
GATAA | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0068others(4): Show | 8 | HG00408.hp2 NA18612.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.1382+6432_1382+643 others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87642908 | |||||
chr6:87642930
|
A | G | 1 | a0001c0002t0001g0342 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1382+6444A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87642930 | ||||||
chr6:87642943
|
T | TAA | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1382+6461_1382+646 others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87642943 | |||||
chr6:87643000
|
A | G | 4 | a0003c0004t0001g0146a0003c0004t0001g0229a0003c0004t0001g0230others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1382+6514A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643000 | ||||||
chr6:87643263
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1382+6777C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643263 | ||||||
chr6:87643298
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1382+6812C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643298 | ||||||
chr6:87643344
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1382+6858G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643344 | ||||||
chr6:87643412
|
T | TA | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0076others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1382+6939dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87643412 | |||||
chr6:87643435
|
G | A | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1382+6949G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643435 | ||||||
chr6:87643445
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1382+6959T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643445 | ||||||
chr6:87643546
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1382+7060G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643546 | ||||||
chr6:87643595
|
A | G | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1382+7109A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643595 | ||||||
chr6:87643601
|
C | G | 37 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(34): Show | 37 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.1382+7115C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643601 | ||||||
chr6:87643829
|
A | T | 2 | a0004c0006t0001g0043a0004c0006t0001g0044 | 2 | NA18990.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1382+7343A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643829 | ||||||
chr6:87643937
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0071 | 2 | NA18984.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1382+7451T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643937 | ||||||
chr6:87643978
|
G | A | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1382+7492G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643978 | ||||||
chr6:87643989
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1382+7503G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87643989 | ||||||
chr6:87644076
|
GTCC | G | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 42 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1382+7592_1382+759 others(7): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644076 | |||||
chr6:87644077
|
TCC | T | 13 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0310others(10): Show | 13 | HG01169.hp1 HG02071.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1382+7592_1382+759 others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644077 | ||||||
chr6:87644078
|
C | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0307a0001c0001t0001g0324 | 3 | HG02572.hp2 HG03540.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1382+7592C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644078 | ||||||
chr6:87644079
|
C | CT | 11 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0025others(8): Show | 13 | HG00733.hp1 HG01433.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1382+7624dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTT | 7 | a0001c0001t0001g0150a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG01081.hp2 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+7621_1382+762 others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0170others(1): Show | 4 | HG02132.hp2 HG02965.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+7615_1382+762 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(4): Show |
2 | a0001c0002t0001g0286a0008c0011t0001g0187 | 2 | HG02258.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1382+7614_1382+762 others(15): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0194 | 3 | HG01928.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1382+7613_1382+762 others(16): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0164 | 2 | HG02615.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1382+7611_1382+762 others(18): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1382+7610_1382+762 others(19): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0118a0001c0001t0001g0195a0001c0002t0001g0290others(1): Show | 4 | HG01943.hp2 HG02895.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+7609_1382+762 others(20): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0148a0003c0004t0001g0146 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1382+7606_1382+762 others(23): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0172 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1382+7605_1382+762 others(24): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0137a0001c0001t0001g0139others(1): Show | 4 | HG02922.hp2 NA18947.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1382+7604_1382+762 others(25): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0215a0003c0004t0001g0230 | 2 | HG02258.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1382+7603_1382+762 others(26): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(16): Show |
7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0132others(4): Show | 7 | HG02735.hp2 HG03130.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1382+7602_1382+762 others(27): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(17): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0197a0001c0001t0001g0212others(3): Show | 7 | HG01261.hp1 HG02257.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+7601_1382+762 others(28): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(18): Show |
11 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0135others(8): Show | 11 | HG00423.hp1 HG01106.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1382+7600_1382+762 others(29): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0221a0001c0001t0001g0223 | 3 | HG01256.hp1 HG01978.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1382+7599_1382+762 others(30): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(20): Show |
7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+7598_1382+762 others(31): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(21): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0200 | 2 | NA18747.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1382+7597_1382+762 others(32): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(22): Show |
4 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01358.hp1 HG01993.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+7596_1382+762 others(33): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(23): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0140a0001c0001t0001g0147others(1): Show | 5 | HG00408.hp1 HG01934.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1382+7595_1382+762 others(34): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(24): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1382+7594_1382+762 others(35): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(25): Show |
4 | a0001c0001t0001g0116a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG03492.hp1 NA18959.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1382+7624_1382+762 others(36): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(27): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0206 | 3 | HG01069.hp2 HG02293.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1382+7624_1382+762 others(38): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(28): Show |
2 | a0001c0001t0001g0188a0001c0001t0005g0129 | 2 | HG01978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1382+7624_1382+762 others(39): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0130 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1382+7624_1382+762 others(40): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(30): Show |
3 | a0001c0001t0001g0165a0001c0001t0001g0207a0006c0009t0001g0190 | 3 | HG00140.hp2 HG03516.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1382+7624_1382+762 others(41): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(32): Show |
1 | a0001c0001t0001g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1382+7624_1382+762 others(43): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
C | CTTTTTTT others(39): Show |
1 | a0001c0001t0001g0167 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1382+7624_1382+762 others(50): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
CT | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(68): Show | 80 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1382+7624delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0186a0001c0001t0001g0219a0001c0001t0001g0232others(3): Show | 6 | HG02055.hp2 HG02056.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1382+7616_1382+762 others(13): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
CTTTTTTT others(3): Show |
C | 34 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(31): Show | 34 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1382+7615_1382+762 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1382+7614_1382+762 others(15): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1382+7612_1382+762 others(17): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644079
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1382+7608_1382+762 others(21): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644079 | |||||
chr6:87644081
|
T | C | 13 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0310others(10): Show | 13 | HG01169.hp1 HG02071.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1382+7595T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644081 | ||||||
chr6:87644082
|
T | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 42 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1382+7596T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644082 | ||||||
chr6:87644083
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1382+7597T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644083 | ||||||
chr6:87644087
|
T | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1382+7601T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644087 | ||||||
chr6:87644233
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1382+7747C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644233 | ||||||
chr6:87644257
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1382+7771T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644257 | ||||||
chr6:87644285
|
G | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1382+7799G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644285 | ||||||
chr6:87644373
|
TA | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(351): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1382+7888delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644373 | ||||||
chr6:87644534
|
G | C | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1382+8048G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644534 | ||||||
chr6:87644551
|
A | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1382+8065A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87644551 | ||||||
chr6:87644847
|
C | CA | 14 | a0001c0001t0001g0181a0001c0001t0002g0006a0001c0001t0002g0013others(11): Show | 17 | HG00280.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1383-8256dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87644847 | |||||
chr6:87645028
|
T | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1383-8088T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645028 | ||||||
chr6:87645040
|
G | A | 1 | a0002c0003t0003g0351 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1383-8076G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645040 | ||||||
chr6:87645119
|
A | G | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 53 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1383-7997A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645119 | ||||||
chr6:87645134
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0310 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1383-7982G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645134 | ||||||
chr6:87645145
|
G | C | 1 | a0001c0005t0002g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1383-7971G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645145 | ||||||
chr6:87645237
|
T | A | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-7879T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645237 | ||||||
chr6:87645254
|
G | C | 1 | a0001c0005t0002g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1383-7862G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645254 | ||||||
chr6:87645318
|
G | A | 2 | a0001c0002t0001g0291a0001c0002t0001g0292 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1383-7798G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645318 | ||||||
chr6:87645347
|
A | G | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-7769A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645347 | ||||||
chr6:87645529
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1383-7587T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645529 | ||||||
chr6:87645670
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1383-7446A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645670 | ||||||
chr6:87645769
|
ACTCCATT others(3): Show |
A | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 55 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1383-7344_1383-733 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87645769 | |||||
chr6:87645843
|
T | A | 1 | a0002c0003t0003g0347 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1383-7273T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645843 | ||||||
chr6:87645888
|
T | A | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-7228T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645888 | ||||||
chr6:87645974
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0098a0001c0001t0001g0318 | 2 | HG02647.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1383-7122_1383-711 others(15): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87645974 | |||||
chr6:87645984
|
C | CT | 34 | a0001c0001t0001g0094a0001c0001t0001g0122a0001c0001t0001g0125others(31): Show | 34 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1383-7122dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87645984 | |||||
chr6:87645994
|
TC | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0282others(2): Show | 5 | HG02145.hp2 HG03209.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383-7121delC | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645994 | ||||||
chr6:87645995
|
C | T | 234 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(231): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1383-7121C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87645995 | ||||||
chr6:87646232
|
C | T | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1383-6884C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87646232 | ||||||
chr6:87646286
|
A | G | 1 | a0001c0002t0001g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1383-6830A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87646286 | ||||||
chr6:87646326
|
TA | T | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 55 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1383-6787delA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87646326 | |||||
chr6:87646680
|
T | C | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1383-6436T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87646680 | ||||||
chr6:87646715
|
T | C | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-6401T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87646715 | ||||||
chr6:87646937
|
C | CT | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1383-6177dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87646937 | |||||
chr6:87647062
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1383-6054C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647062 | ||||||
chr6:87647187
|
C | T | 4 | a0001c0002t0001g0285a0001c0002t0001g0286a0001c0002t0001g0293others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383-5929C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647187 | ||||||
chr6:87647197
|
G | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1383-5919G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647197 | ||||||
chr6:87647233
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1383-5883C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647233 | ||||||
chr6:87647242
|
T | C | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-5874T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647242 | ||||||
chr6:87647353
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1383-5763T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647353 | ||||||
chr6:87647412
|
G | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1383-5704G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647412 | ||||||
chr6:87647454
|
C | T | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1383-5662C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647454 | ||||||
chr6:87647483
|
A | C | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0009c0013t0001g0337 | 3 | HG02145.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1383-5633A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647483 | ||||||
chr6:87647541
|
C | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1383-5575C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647541 | ||||||
chr6:87647558
|
C | T | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1383-5558C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647558 | ||||||
chr6:87647580
|
T | G | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | NA18971.hp2 NA18982.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1383-5536T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647580 | ||||||
chr6:87647663
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1383-5453A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647663 | ||||||
chr6:87647864
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1383-5252G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647864 | ||||||
chr6:87647909
|
A | G | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1383-5207A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647909 | ||||||
chr6:87647966
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1383-5150G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87647966 | ||||||
chr6:87648031
|
G | C | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1383-5085G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648031 | ||||||
chr6:87648074
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1383-5042G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648074 | ||||||
chr6:87648200
|
A | AAAAAC | 3 | a0001c0001t0001g0127a0001c0001t0001g0155a0001c0001t0001g0306 | 3 | HG00597.hp2 HG03471.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1383-4890_1383-488 others(9): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87648200 | |||||
chr6:87648200
|
A | AAAAACAA others(3): Show |
1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1383-4895_1383-488 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87648200 | |||||
chr6:87648200
|
AAAAACAA others(3): Show |
A | 2 | a0003c0004t0001g0229a0003c0004t0001g0230 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1383-4895_1383-488 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87648200 | |||||
chr6:87648624
|
G | T | 1 | a0001c0002t0001g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1383-4492G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648624 | ||||||
chr6:87648668
|
T | TATTGATA others(3): Show |
20 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(17): Show | 20 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1383-4448_1383-444 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648668 | ||||||
chr6:87648668
|
T | TATTGATA others(3): Show |
1 | a0001c0002t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1383-4448_1383-444 others(14): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648668 | ||||||
chr6:87648693
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0009c0013t0001g0337 | 3 | HG02145.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1383-4423C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648693 | ||||||
chr6:87648772
|
C | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1383-4344C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648772 | ||||||
chr6:87648950
|
A | G | 3 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1383-4166A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87648950 | ||||||
chr6:87649361
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1383-3755T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87649361 | ||||||
chr6:87649473
|
C | T | 1 | a0002c0003t0003g0343 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1383-3643C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87649473 | ||||||
chr6:87649709
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1383-3407G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87649709 | ||||||
chr6:87649826
|
G | C | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1383-3290G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87649826 | ||||||
chr6:87649980
|
A | G | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-3136A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87649980 | ||||||
chr6:87650041
|
CACTT | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1383-3070_1383-306 others(8): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87650041 | |||||
chr6:87650061
|
C | CT | 78 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(75): Show | 82 | HG00323.hp1 HG00597.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1383-3038dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87650061 | |||||
chr6:87650061
|
CT | C | 7 | a0001c0001t0001g0093a0001c0001t0001g0118a0001c0001t0001g0141others(4): Show | 7 | HG02809.hp1 HG02897.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1383-3038delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87650061 | |||||
chr6:87650113
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0295a0001c0001t0001g0299others(8): Show | 12 | HG00735.hp2 HG01106.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1383-3003A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650113 | ||||||
chr6:87650142
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1383-2974G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650142 | ||||||
chr6:87650258
|
G | A | 1 | a0003c0004t0006g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1383-2858G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650258 | ||||||
chr6:87650306
|
G | A | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1383-2810G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650306 | ||||||
chr6:87650569
|
A | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1383-2547A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650569 | ||||||
chr6:87650715
|
TAAG | T | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-2399_1383-239 others(7): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87650715 | |||||
chr6:87650776
|
G | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1383-2340G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650776 | ||||||
chr6:87650863
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1383-2253C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650863 | ||||||
chr6:87650928
|
AC | A | 57 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(54): Show | 61 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1383-2186delC | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87650928 | |||||
chr6:87650956
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1383-2160G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650956 | ||||||
chr6:87650964
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1383-2152G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650964 | ||||||
chr6:87650984
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1383-2132G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87650984 | ||||||
chr6:87651003
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1383-2113G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651003 | ||||||
chr6:87651018
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1383-2098C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651018 | ||||||
chr6:87651018
|
C | G | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 53 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1383-2098C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651018 | ||||||
chr6:87651121
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1383-1995C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651121 | ||||||
chr6:87651133
|
T | C | 3 | a0001c0002t0001g0290a0001c0002t0001g0291a0001c0002t0001g0292 | 3 | HG02895.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1383-1983T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651133 | ||||||
chr6:87651157
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1383-1959G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651157 | ||||||
chr6:87651239
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1383-1877C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651239 | ||||||
chr6:87651299
|
G | A | 163 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0097others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1383-1817G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651299 | ||||||
chr6:87651337
|
C | T | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-1779C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651337 | ||||||
chr6:87651338
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1383-1778G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651338 | ||||||
chr6:87651621
|
C | T | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1383-1495C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87651621 | ||||||
chr6:87651901
|
C | CT | 52 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 56 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1383-1200dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 87651901 | |||||
chr6:87652023
|
C | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1383-1093C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652023 | ||||||
chr6:87652055
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1383-1061C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652055 | ||||||
chr6:87652102
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1383-1014G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652102 | ||||||
chr6:87652158
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1383-958A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652158 | ||||||
chr6:87652163
|
G | A | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 60 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1383-953G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652163 | ||||||
chr6:87652448
|
A | G | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1383-668A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652448 | ||||||
chr6:87652625
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1383-491G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652625 | ||||||
chr6:87652956
|
A | G | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 52 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1383-160A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87652956 | ||||||
chr6:87653025
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1383-91C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 13/19 | chr6 | 87653025 | ||||||
chr6:87653494
|
T | C | 40 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(37): Show | 40 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1516+245T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87653494 | ||||||
chr6:87653750
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1516+501C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87653750 | ||||||
chr6:87653812
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0233 | 2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1516+563C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87653812 | ||||||
chr6:87653854
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1516+605A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87653854 | ||||||
chr6:87653922
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1516+673A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87653922 | ||||||
chr6:87654091
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1516+842A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87654091 | ||||||
chr6:87654095
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1516+846A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87654095 | ||||||
chr6:87654615
|
T | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | NA18971.hp2 NA18982.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1516+1366T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87654615 | ||||||
chr6:87654636
|
A | G | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1516+1387A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87654636 | ||||||
chr6:87654753
|
G | A | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1516+1504G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87654753 | ||||||
chr6:87655073
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1516+1824G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655073 | ||||||
chr6:87655098
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517-1808A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655098 | ||||||
chr6:87655120
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1517-1786C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655120 | ||||||
chr6:87655353
|
A | AT | 157 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(154): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1517-1536dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 87655353 | |||||
chr6:87655353
|
A | ATT | 8 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 8 | HG00597.hp2 HG02886.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1517-1537_1517-153 others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 87655353 | |||||
chr6:87655460
|
T | G | 1 | a0001c0001t0001g0271 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1517-1446T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655460 | ||||||
chr6:87655573
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02080.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1517-1333G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655573 | ||||||
chr6:87655666
|
A | T | 6 | a0001c0001t0001g0331a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 6 | HG02109.hp2 HG02486.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1517-1240A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655666 | ||||||
chr6:87655666
|
AT | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0114others(4): Show | 7 | HG01070.hp2 HG01167.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-1226delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 87655666 | |||||
chr6:87655669
|
T | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(80): Show | 86 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.1517-1237T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655669 | ||||||
chr6:87655672
|
T | A | 7 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(4): Show | 7 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-1234T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655672 | ||||||
chr6:87655675
|
T | A | 2 | a0003c0004t0001g0229a0003c0004t0001g0230 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1517-1231T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655675 | ||||||
chr6:87655721
|
C | T | 1 | a0001c0002t0001g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1517-1185C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655721 | ||||||
chr6:87655728
|
C | T | 21 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1517-1178C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655728 | ||||||
chr6:87655927
|
T | G | 4 | a0003c0004t0001g0146a0003c0004t0001g0229a0003c0004t0001g0230others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-979T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87655927 | ||||||
chr6:87656115
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1517-791G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656115 | ||||||
chr6:87656192
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18963.hp2 NA18966.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-714C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656192 | ||||||
chr6:87656271
|
A | G | 1 | a0008c0011t0001g0187 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1517-635A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656271 | ||||||
chr6:87656353
|
C | T | 12 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517-553C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656353 | ||||||
chr6:87656358
|
C | T | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1517-548C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656358 | ||||||
chr6:87656359
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517-547G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656359 | ||||||
chr6:87656360
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517-546G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656360 | ||||||
chr6:87656362
|
TG | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517-542delG | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 87656362 | |||||
chr6:87656404
|
G | A | 45 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 49 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1517-502G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656404 | ||||||
chr6:87656441
|
A | C | 1 | a0003c0004t0001g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1517-465A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656441 | ||||||
chr6:87656482
|
G | A | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1517-424G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656482 | ||||||
chr6:87656551
|
C | T | 4 | a0003c0004t0001g0146a0003c0004t0001g0229a0003c0004t0001g0230others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-355C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656551 | ||||||
chr6:87656597
|
A | AT | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1517-298dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 87656597 | |||||
chr6:87656598
|
T | A | 21 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1517-308T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656598 | ||||||
chr6:87656775
|
G | T | 1 | a0003c0004t0006g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1517-131G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656775 | ||||||
chr6:87656825
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1517-81T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656825 | ||||||
chr6:87656884
|
A | G | 125 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0116others(122): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1517-22A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 14/19 | chr6 | 87656884 | ||||||
chr6:87656990
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(116): Show | 133 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(130): Show |
splice_region_variant&intron_variant | LOW | c.1593+8C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87656990 | ||||||
chr6:87657053
|
A | G | 245 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(242): Show | 251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1593+71A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657053 | ||||||
chr6:87657066
|
GT | G | 13 | a0001c0001t0001g0273a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1593+89delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr6 | 87657066 | |||||
chr6:87657150
|
T | C | 16 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 16 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1593+168T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657150 | ||||||
chr6:87657363
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01109.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1593+381T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657363 | ||||||
chr6:87657364
|
C | T | 236 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(233): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1593+382C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657364 | ||||||
chr6:87657690
|
T | C | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1594-231T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657690 | ||||||
chr6:87657808
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1594-113T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657808 | ||||||
chr6:87657841
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1594-80A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657841 | ||||||
chr6:87657842
|
T | C | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1594-79T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657842 | ||||||
chr6:87657917
|
A | G | 36 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(33): Show | 36 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(33): Show |
splice_region_variant&intron_variant | LOW | c.1594-4A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 15/19 | chr6 | 87657917 | ||||||
chr6:87658200
|
G | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0040a0001c0001t0002g0100others(4): Show | 7 | HG01884.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1691+182G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658200 | ||||||
chr6:87658282
|
C | G | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1691+264C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658282 | ||||||
chr6:87658412
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1691+394G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658412 | ||||||
chr6:87658440
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1691+422G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658440 | ||||||
chr6:87658456
|
C | CA | 168 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(165): Show | 174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1691+452dupA | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87658456 | |||||
chr6:87658608
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1691+590G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658608 | ||||||
chr6:87658613
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1691+595T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658613 | ||||||
chr6:87658645
|
G | A | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1691+627G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658645 | ||||||
chr6:87658732
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1691+714A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658732 | ||||||
chr6:87658946
|
T | C | 3 | a0001c0001t0001g0300a0001c0001t0001g0302a0001c0001t0001g0334 | 3 | HG02809.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1691+928T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658946 | ||||||
chr6:87658964
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1691+946C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87658964 | ||||||
chr6:87659022
|
C | CG | 39 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0149others(36): Show | 39 | HG00099.hp1 HG01069.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1691+1013dupG | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87659022 | |||||
chr6:87659022
|
C | G | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1691+1004C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659022 | ||||||
chr6:87659025
|
G | C | 1 | a0001c0001t0001g0332 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1691+1007G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659025 | ||||||
chr6:87659025
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1691+1007G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659025 | ||||||
chr6:87659027
|
G | T | 1 | a0002c0003t0003g0343 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1691+1009G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659027 | ||||||
chr6:87659029
|
G | C | 7 | a0001c0001t0001g0220a0001c0001t0001g0224a0001c0002t0001g0285others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1691+1011G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659029 | ||||||
chr6:87659029
|
G | GC | 5 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG02886.hp2 HG03486.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1691+1011_1691+101 others(5): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659029 | ||||||
chr6:87659058
|
A | AT | 25 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0045others(22): Show | 25 | HG00423.hp1 HG00597.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1691+1063dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87659058 | |||||
chr6:87659058
|
AT | A | 29 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0141others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1691+1063delT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87659058 | |||||
chr6:87659058
|
ATT | A | 24 | a0001c0001t0001g0258a0001c0001t0001g0261a0001c0001t0001g0267others(21): Show | 27 | HG01891.hp1 HG02055.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.1691+1062_1691+106 others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87659058 | |||||
chr6:87659058
|
ATTT | A | 47 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0162others(44): Show | 47 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.1691+1061_1691+106 others(7): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87659058 | |||||
chr6:87659084
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1691+1066G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659084 | ||||||
chr6:87659149
|
C | T | 3 | a0001c0001t0001g0300a0001c0001t0001g0302a0001c0001t0001g0334 | 3 | HG02809.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1691+1131C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659149 | ||||||
chr6:87659246
|
T | G | 19 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0022others(16): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1691+1228T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659246 | ||||||
chr6:87659314
|
G | A | 36 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(33): Show | 36 | HG01074.hp1 HG01167.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1691+1296G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659314 | ||||||
chr6:87659476
|
A | G | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1691+1458A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659476 | ||||||
chr6:87659551
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1691+1533T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659551 | ||||||
chr6:87659604
|
G | A | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1691+1586G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659604 | ||||||
chr6:87659650
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1691+1632G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659650 | ||||||
chr6:87659676
|
G | A | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1691+1658G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659676 | ||||||
chr6:87659727
|
C | T | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 53 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1691+1709C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659727 | ||||||
chr6:87659794
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1691+1776A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659794 | ||||||
chr6:87659806
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1691+1788C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659806 | ||||||
chr6:87659812
|
G | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1691+1794G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87659812 | ||||||
chr6:87659940
|
A | ATTT | 252 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(249): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1691+1923_1691+192 others(7): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87659940 | |||||
chr6:87660023
|
T | C | 1 | a0001c0002t0001g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1691+2005T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660023 | ||||||
chr6:87660125
|
G | A | 43 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(40): Show | 43 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1691+2107G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660125 | ||||||
chr6:87660197
|
C | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0137a0001c0001t0001g0233 | 3 | NA18971.hp1 NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1691+2179C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660197 | ||||||
chr6:87660507
|
T | C | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1691+2489T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660507 | ||||||
chr6:87660602
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1692-2401G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660602 | ||||||
chr6:87660634
|
A | C | 252 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(249): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1692-2369A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660634 | ||||||
chr6:87660878
|
C | T | 19 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0022others(16): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1692-2125C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87660878 | ||||||
chr6:87661046
|
C | G | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692-1957C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661046 | ||||||
chr6:87661078
|
G | GT | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1692-1922dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87661078 | |||||
chr6:87661141
|
G | C | 41 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(38): Show | 41 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.1692-1862G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661141 | ||||||
chr6:87661178
|
TATA | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0206a0001c0001t0001g0216others(1): Show | 4 | HG00099.hp1 HG01243.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692-1822_1692-182 others(7): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 87661178 | |||||
chr6:87661239
|
C | A | 50 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 54 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1692-1764C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661239 | ||||||
chr6:87661342
|
T | C | 252 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(249): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1692-1661T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661342 | ||||||
chr6:87661418
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1692-1585G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661418 | ||||||
chr6:87661462
|
G | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1692-1541G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661462 | ||||||
chr6:87661698
|
C | T | 19 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0022others(16): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1692-1305C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661698 | ||||||
chr6:87661722
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0001g0180 | 3 | HG01069.hp2 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1692-1281A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661722 | ||||||
chr6:87661730
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1692-1273T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661730 | ||||||
chr6:87661850
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1692-1153C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661850 | ||||||
chr6:87661967
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1692-1036G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87661967 | ||||||
chr6:87662022
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1692-981A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662022 | ||||||
chr6:87662123
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1692-880C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662123 | ||||||
chr6:87662135
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0007g0032 | 3 | HG01517.hp2 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1692-868A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662135 | ||||||
chr6:87662281
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0009c0013t0001g0337 | 3 | HG02145.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1692-722C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662281 | ||||||
chr6:87662285
|
C | T | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1692-718C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662285 | ||||||
chr6:87662381
|
G | A | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692-622G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662381 | ||||||
chr6:87662430
|
C | G | 1 | a0001c0002t0001g0340 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1692-573C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662430 | ||||||
chr6:87662441
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1692-562C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662441 | ||||||
chr6:87662446
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0249 | 2 | NA18995.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1692-557A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662446 | ||||||
chr6:87662474
|
A | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1692-529A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662474 | ||||||
chr6:87662476
|
G | A | 1 | a0001c0002t0001g0340 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1692-527G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662476 | ||||||
chr6:87662528
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1692-475A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662528 | ||||||
chr6:87662543
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1692-460A>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662543 | ||||||
chr6:87662933
|
T | A | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1692-70T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 16/19 | chr6 | 87662933 | ||||||
chr6:87663154
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1833+10A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663154 | ||||||
chr6:87663266
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0074 | 2 | NA18612.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1833+122G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663266 | ||||||
chr6:87663818
|
A | G | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1833+674A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663818 | ||||||
chr6:87663892
|
T | G | 19 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0022others(16): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1833+748T>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663892 | ||||||
chr6:87663933
|
G | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0009c0013t0001g0337 | 3 | HG02145.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1833+789G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663933 | ||||||
chr6:87663959
|
A | G | 19 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0022others(16): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1834-784A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663959 | ||||||
chr6:87663976
|
G | C | 1 | a0010c0007t0001g0352 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1834-767G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87663976 | ||||||
chr6:87664002
|
G | T | 1 | a0001c0001t0001g0319 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1834-741G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664002 | ||||||
chr6:87664006
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1834-737A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664006 | ||||||
chr6:87664069
|
A | G | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1834-674A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664069 | ||||||
chr6:87664166
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1834-577A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664166 | ||||||
chr6:87664198
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1834-545G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664198 | ||||||
chr6:87664433
|
T | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02886.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1834-310T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664433 | ||||||
chr6:87664633
|
A | G | 2 | a0001c0002t0001g0285a0001c0002t0001g0286 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1834-110A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 17/19 | chr6 | 87664633 | ||||||
chr6:87664940
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1950+81G>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 18/19 | chr6 | 87664940 | ||||||
chr6:87665095
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+236C>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 18/19 | chr6 | 87665095 | ||||||
chr6:87665178
|
C | A | 1 | a0001c0002t0001g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1950+319C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 18/19 | chr6 | 87665178 | ||||||
chr6:87665525
|
C | CTTGT | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1951-227_1951-226i others(6): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 87665525 | |||||
chr6:87665620
|
G | A | 13 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1951-134G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 18/19 | chr6 | 87665620 | ||||||
chr6:87666041
|
G | C | 12 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0103others(9): Show | 15 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2030+208G>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666041 | ||||||
chr6:87666195
|
G | A | 9 | a0002c0003t0003g0343a0002c0003t0003g0344a0002c0003t0003g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2030+362G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666195 | ||||||
chr6:87666215
|
T | A | 1 | a0001c0002t0001g0290 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2030+382T>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666215 | ||||||
chr6:87666280
|
T | C | 11 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0104others(8): Show | 14 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2030+447T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666280 | ||||||
chr6:87666293
|
A | AGCTAATT others(182): Show |
1 | a0001c0001t0001g0353 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2030+478_2030+479i others(191): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 87666293 | |||||
chr6:87666321
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2030+488G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666321 | ||||||
chr6:87666332
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2030+499A>G | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666332 | ||||||
chr6:87666337
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2030+504G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666337 | ||||||
chr6:87666342
|
G | A | 1 | a0001c0002t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2030+509G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666342 | ||||||
chr6:87666344
|
C | A | 5 | a0001c0001t0001g0160a0001c0001t0001g0282a0001c0001t0001g0283others(2): Show | 5 | HG00597.hp1 HG01081.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2030+511C>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666344 | ||||||
chr6:87666352
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG00099.hp2 HG00140.hp1 |
intron_variant | MODIFIER | c.2030+519G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666352 | ||||||
chr6:87666435
|
C | CT | 51 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0102others(48): Show | 51 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.2031-563dupT | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 87666435 | |||||
chr6:87666435
|
C | CTT | 22 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0022others(19): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2031-564_2031-563d others(4): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 87666435 | |||||
chr6:87666435
|
C | CTTT | 17 | a0001c0001t0001g0154a0001c0001t0001g0296a0001c0001t0001g0297others(14): Show | 17 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2031-565_2031-563d others(5): Show |
ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 87666435 | |||||
chr6:87666501
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2031-517C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666501 | ||||||
chr6:87666572
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2031-446G>A | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666572 | ||||||
chr6:87666583
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | NA19057.hp2 NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2031-435C>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666583 | ||||||
chr6:87666787
|
A | T | 1 | a0007c0010t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2031-231A>T | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666787 | ||||||
chr6:87666839
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2031-179T>C | ORC3 | ENSG00000135336.16 | transcript | ENST00000392844.8 | protein_coding | 19/19 | chr6 | 87666839 |