geneid | 5000 |
---|---|
ensemblid | ENSG00000115947.14 |
hgncid | 8490 |
symbol | ORC4 |
name | origin recognition complex subunit 4 |
refseq_nuc | NM_181741.4 |
refseq_prot | NP_859525.1 |
ensembl_nuc | ENST00000392857.10 |
ensembl_prot | ENSP00000376597.5 |
mane_status | MANE Select |
chr | chr2 |
start | 147930396 |
end | 148020737 |
strand | - |
ver | v1.2 |
region | chr2:147930396-148020737 |
region5000 | chr2:147925396-148025737 |
regionname0 | ORC4_chr2_147930396_148020737 |
regionname5000 | ORC4_chr2_147925396_148025737 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 436 | 194 | 61 | 31 | 74 | 5 | 21 | 57 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002 | 0/0 | 436 | 132 | 20 | 31 | 58 | 6 | 17 | 46 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0003 | 0/0 | 436 | 7 | 2 | 2 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0004 | 0/0 | 436 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0005 | 0/0 | 436 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1311 | 192 | 59 | 31 | 74 | 5 | 21 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
c0002 | 0/0 | 1311 | 132 | 20 | 31 | 58 | 6 | 17 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
c0003 | 0/0 | 1311 | 7 | 2 | 2 | 0 | 3 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
c0004 | 0/0 | 1311 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
c0005 | 0/0 | 1311 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
c0006 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5237 | 80 | 1 | 13 | 50 | 4 | 12 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0002 | 0/0 | 5236 | 77 | 5 | 13 | 43 | 5 | 11 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0003 | 0/1 | 5237 | 36 | 3 | 7 | 17 | 0 | 8 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0004 | 0/0 | 5236 | 24 | 3 | 13 | 8 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0005 | 1/0 | 5237 | 13 | 6 | 5 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0006 | 0/0 | 5237 | 7 | 7 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0007 | 0/0 | 5236 | 6 | 6 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0008 | 0/0 | 5236 | 6 | 5 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0009 | 0/0 | 5237 | 5 | 1 | 1 | 1 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0010 | 0/0 | 5237 | 5 | 5 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0011 | 0/0 | 5237 | 5 | 2 | 2 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0012 | 0/0 | 5239 | 4 | 1 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0013 | 0/0 | 5236 | 4 | 0 | 2 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0014 | 0/0 | 5240 | 4 | 4 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0015 | 0/0 | 5240 | 3 | 1 | 1 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0016 | 0/0 | 5240 | 3 | 3 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0017 | 0/0 | 5236 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0018 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0019 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0020 | 0/0 | 5237 | 2 | 0 | 0 | 0 | 2 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0021 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0022 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0023 | 0/0 | 5238 | 2 | 0 | 0 | 1 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0024 | 0/0 | 5237 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0025 | 0/0 | 5236 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0026 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0027 | 0/0 | 5236 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0028 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0029 | 0/0 | 5236 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0030 | 0/0 | 5236 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0031 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0032 | 0/0 | 5236 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0033 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0034 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0035 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0036 | 0/0 | 5236 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0037 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0038 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0039 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0040 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0041 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0042 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0043 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0044 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0045 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0046 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0047 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0048 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0049 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0050 | 0/0 | 5236 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0051 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0052 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0053 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0054 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0055 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0056 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0057 | 0/0 | 5239 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0058 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0059 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0060 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0061 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
t0062 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1311 | 192 | 59 | 31 | 74 | 5 | 21 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0004 | 0/0 | 1311 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002 | 0/0 | 1311 | 132 | 20 | 31 | 58 | 6 | 17 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0003c0003 | 0/0 | 1311 | 7 | 2 | 2 | 0 | 3 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0004c0005 | 0/0 | 1311 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0005c0006 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6547 | 78 | 1 | 13 | 48 | 4 | 12 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0003 | 0/1 | 6547 | 36 | 3 | 7 | 17 | 0 | 8 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0005 | 1/0 | 6547 | 13 | 6 | 5 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0006 | 0/0 | 6547 | 6 | 6 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0007 | 0/0 | 6546 | 5 | 5 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0008 | 0/0 | 6546 | 6 | 5 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0012 | 0/0 | 6549 | 4 | 1 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0014 | 0/0 | 6550 | 4 | 4 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0016 | 0/0 | 6550 | 3 | 3 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0018 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0019 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0021 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0022 | 0/0 | 6547 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0023 | 0/0 | 6548 | 2 | 0 | 0 | 1 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0024 | 0/0 | 6547 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0026 | 0/0 | 6549 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0028 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0035 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0041 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0042 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0043 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0044 | 0/0 | 6547 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0045 | 0/0 | 6547 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0046 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0047 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0048 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0049 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0050 | 0/0 | 6546 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0051 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0052 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0053 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0054 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0055 | 0/0 | 6549 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0056 | 0/0 | 6550 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0057 | 0/0 | 6549 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0058 | 0/0 | 6548 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0059 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0060 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0061 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0001t0062 | 0/0 | 6547 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0004t0006 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0001c0004t0007 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0002 | 0/0 | 6546 | 77 | 5 | 13 | 43 | 5 | 11 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0004 | 0/0 | 6546 | 24 | 3 | 13 | 8 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0009 | 0/0 | 6547 | 5 | 1 | 1 | 1 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0010 | 0/0 | 6547 | 5 | 5 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0013 | 0/0 | 6546 | 4 | 0 | 2 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0015 | 0/0 | 6550 | 3 | 1 | 1 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0017 | 0/0 | 6546 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0025 | 0/0 | 6546 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0027 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0029 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0030 | 0/0 | 6546 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0031 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0032 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0033 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0034 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0036 | 0/0 | 6546 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0038 | 0/0 | 6547 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0039 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0002c0002t0040 | 0/0 | 6547 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0003c0003t0011 | 0/0 | 6547 | 5 | 2 | 2 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0003c0003t0020 | 0/0 | 6547 | 2 | 0 | 0 | 0 | 2 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0004c0005t0001 | 0/0 | 6547 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
a0005c0006t0037 | 0/0 | 6546 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | copy fasta | chr2 | 147925396 | 148025737 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0006g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0008g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0012g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0012g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0016g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0018g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0018g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0019g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0019g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0021g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0022g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0022g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0023g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0023g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0024g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0024g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0026g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0028g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0035g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0041g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0042g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0043g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0044g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0045g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0046g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0047g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0048g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0049g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0050g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0051g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0052g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0053g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0054g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0055g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0056g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0057g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0058g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0059g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0060g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0061g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0001t0062g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0004t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0001c0004t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0009g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0010g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0013g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0013g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0013g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0013g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0015g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0015g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0017g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0025g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0027g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0029g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0030g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0031g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0032g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0033g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0034g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0036g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0038g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0039g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0002c0002t0040g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0011g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0011g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0011g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0020g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0003c0003t0020g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0004c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0004c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
a0005c0006t0037g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0084 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00099 | hp2 | a0003 | c0003 | t0011 | g0239 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00140 | hp1 | a0002 | c0002 | t0015 | g0078 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0080 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0129 | EUR | FIN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00408 | hp1 | a0001 | c0001 | t0012 | g0022 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00423 | hp2 | a0002 | c0002 | t0004 | g0040 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00558 | hp2 | a0002 | c0002 | t0009 | g0132 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00642 | hp1 | a0002 | c0002 | t0013 | g0073 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00673 | hp2 | a0004 | c0005 | t0001 | g0172 | EAS | CHS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00733 | hp2 | a0001 | c0001 | t0044 | g0278 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0094 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00738 | hp2 | a0002 | c0002 | t0004 | g0038 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01106 | hp1 | a0001 | c0001 | t0045 | g0280 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01109 | hp1 | a0003 | c0003 | t0011 | g0233 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0257 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01168 | hp1 | a0001 | c0001 | t0024 | g0191 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01168 | hp2 | a0003 | c0003 | t0011 | g0235 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01169 | hp1 | a0001 | c0001 | t0024 | g0192 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01175 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01256 | hp1 | a0002 | c0002 | t0013 | g0058 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01261 | hp1 | a0001 | c0001 | t0050 | g0244 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01261 | hp2 | a0002 | c0002 | t0004 | g0061 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0181 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01516 | hp2 | a0003 | c0003 | t0020 | g0237 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0114 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01517 | hp2 | a0003 | c0003 | t0020 | g0238 | EUR | IBS | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01884 | hp1 | a0002 | c0002 | t0015 | g0077 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01891 | hp1 | a0001 | c0004 | t0007 | g0268 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0305 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01928 | hp1 | a0002 | c0002 | t0004 | g0037 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01934 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01934 | hp2 | a0002 | c0002 | t0009 | g0110 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01943 | hp1 | a0002 | c0002 | t0004 | g0046 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01975 | hp2 | a0002 | c0002 | t0004 | g0137 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01978 | hp1 | a0002 | c0002 | t0004 | g0026 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01981 | hp2 | a0002 | c0002 | t0004 | g0028 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0034 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02055 | hp1 | a0002 | c0002 | t0033 | g0032 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02071 | hp1 | a0001 | c0001 | t0060 | g0294 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02145 | hp1 | a0001 | c0001 | t0052 | g0164 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02145 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CDX | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0265 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02258 | hp1 | a0002 | c0002 | t0031 | g0066 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0252 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02273 | hp1 | a0002 | c0002 | t0025 | g0036 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02293 | hp1 | a0002 | c0002 | t0004 | g0118 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02300 | hp1 | a0002 | c0002 | t0004 | g0024 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02300 | hp2 | a0002 | c0002 | t0015 | g0076 | AMR | PEL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02523 | hp2 | a0002 | c0002 | t0036 | g0123 | EAS | KHV | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02615 | hp1 | a0001 | c0001 | t0019 | g0301 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02622 | hp1 | a0001 | c0001 | t0053 | g0226 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02622 | hp2 | a0002 | c0002 | t0010 | g0049 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0161 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02630 | hp2 | a0001 | c0001 | t0054 | g0175 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02647 | hp1 | a0001 | c0001 | t0014 | g0160 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02647 | hp2 | a0001 | c0004 | t0006 | g0266 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02683 | hp1 | a0002 | c0002 | t0038 | g0031 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0249 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02738 | hp2 | a0002 | c0002 | t0013 | g0060 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02809 | hp2 | a0001 | c0001 | t0059 | g0158 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02818 | hp1 | a0001 | c0001 | t0018 | g0264 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02818 | hp2 | a0001 | c0001 | t0058 | g0250 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02886 | hp1 | a0001 | c0001 | t0055 | g0261 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02886 | hp2 | a0002 | c0002 | t0010 | g0050 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02895 | hp1 | a0002 | c0002 | t0010 | g0005 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02895 | hp2 | a0002 | c0002 | t0004 | g0030 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02896 | hp2 | a0001 | c0001 | t0021 | g0187 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02897 | hp1 | a0001 | c0001 | t0021 | g0306 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02897 | hp2 | a0002 | c0002 | t0010 | g0005 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02922 | hp1 | a0001 | c0001 | t0041 | g0234 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0304 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02965 | hp2 | a0002 | c0002 | t0010 | g0048 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02976 | hp1 | a0001 | c0001 | t0016 | g0303 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0256 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0283 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03098 | hp1 | a0002 | c0002 | t0009 | g0052 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03098 | hp2 | a0001 | c0001 | t0048 | g0259 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03139 | hp1 | a0002 | c0002 | t0004 | g0029 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03139 | hp2 | a0001 | c0001 | t0014 | g0163 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0254 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03453 | hp1 | a0001 | c0001 | t0057 | g0162 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03453 | hp2 | a0001 | c0001 | t0022 | g0267 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03486 | hp1 | a0001 | c0001 | t0051 | g0260 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03486 | hp2 | a0001 | c0001 | t0022 | g0251 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03490 | hp2 | a0002 | c0002 | t0013 | g0136 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0085 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03516 | hp1 | a0001 | c0001 | t0026 | g0018 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | ESN | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03669 | hp1 | a0001 | c0001 | t0023 | g0195 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0088 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03831 | hp2 | a0002 | c0002 | t0030 | g0059 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0100 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0281 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0079 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0075 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04115 | hp1 | a0002 | c0002 | t0009 | g0092 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | BEB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04204 | hp2 | a0002 | c0002 | t0009 | g0091 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | STU | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18522 | hp1 | a0001 | c0001 | t0049 | g0263 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | CHB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | CHB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18942 | hp2 | a0002 | c0002 | t0017 | g0008 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18944 | hp2 | a0001 | c0001 | t0061 | g0220 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18945 | hp1 | a0002 | c0002 | t0017 | g0008 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18946 | hp1 | a0001 | c0001 | t0043 | g0299 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18959 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18969 | hp2 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18971 | hp2 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18972 | hp2 | a0004 | c0005 | t0001 | g0219 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18974 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18984 | hp1 | a0002 | c0002 | t0004 | g0041 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18985 | hp1 | a0002 | c0002 | t0027 | g0096 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18986 | hp1 | a0002 | c0002 | t0032 | g0057 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18987 | hp1 | a0002 | c0002 | t0004 | g0042 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18994 | hp1 | a0001 | c0001 | t0023 | g0223 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19005 | hp1 | a0001 | c0001 | t0062 | g0188 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19010 | hp1 | a0002 | c0002 | t0029 | g0138 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19030 | hp2 | a0001 | c0001 | t0035 | g0025 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19043 | hp2 | a0001 | c0001 | t0046 | g0262 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19075 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19079 | hp1 | a0001 | c0001 | t0028 | g0112 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19082 | hp2 | a0002 | c0002 | t0004 | g0033 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19087 | hp2 | a0002 | c0002 | t0004 | g0134 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19240 | hp1 | a0005 | c0006 | t0037 | g0047 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA19240 | hp2 | a0002 | c0002 | t0040 | g0140 | AFR | YRI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA20129 | hp1 | a0001 | c0001 | t0056 | g0165 | AFR | ASW | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA20129 | hp2 | a0001 | c0001 | t0047 | g0258 | AFR | ASW | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0072 | EUR | TSI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0316 | EUR | TSI | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01123 | hp1 | a0002 | c0002 | t0004 | g0043 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0115 | AMR | CLM | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02109 | hp1 | a0002 | c0002 | t0034 | g0039 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0247 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG02486 | hp2 | a0001 | c0001 | t0042 | g0255 | AFR | ACB | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03471 | hp1 | a0002 | c0002 | t0039 | g0139 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | MSL | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG06807 | hp1 | a0003 | c0003 | t0011 | g0143 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA20300 | hp1 | a0001 | c0001 | t0019 | g0302 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA20300 | hp2 | a0002 | c0002 | t0004 | g0125 | AFR | USA | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA21309 | hp1 | a0003 | c0003 | t0011 | g0236 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0023 | AFR | LWK | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0279 | REF | REF | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0186 | REF | REF | ORC4_chr2_147925396_148025737 | ORC4 | chr2 | 147925396 | 148025737 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:147948209
|
A | C | 1 | a0005 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.604T>G | p.Leu202Val | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/14 | 726/6547 | 604/1311 | 202/436 | chr2 | 147948209 | ||
chr2:147958805
|
T | C | 1 | a0004 | 2 | HG00673.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.287A>G | p.Gln96Arg | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/14 | 409/6547 | 287/1311 | 96/436 | chr2 | 147958805 | ||
chr2:147958859
|
T | C | 2 | a0002a0005 | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
missense_variant | MODERATE | c.233A>G | p.Asn78Ser | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/14 | 355/6547 | 233/1311 | 78/436 | chr2 | 147958859 | ||
chr2:147972798
|
G | C | 1 | a0003 | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
missense_variant | MODERATE | c.166C>G | p.Leu56Val | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/14 | 288/6547 | 166/1311 | 56/436 | chr2 | 147972798 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:147938389
|
T | C | 1 | a0001c0004 | 2 | HG01891.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.963A>G | p.Leu321Leu | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 12/14 | 1085/6547 | 963/1311 | 321/436 | chr2 | 147938389 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:147930513
|
T | C | 1 | a0001c0001t0053 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4997A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4997 | chr2 | 147930513 | |||||
chr2:147930605
|
A | G | 1 | a0002c0002t0031 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4905T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4905 | chr2 | 147930605 | |||||
chr2:147930614
|
T | C | 1 | a0001c0001t0050 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4896A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4896 | chr2 | 147930614 | |||||
chr2:147930821
|
G | A | 2 | a0001c0001t0054a0002c0002t0031 | 2 | HG02258.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4689C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4689 | chr2 | 147930821 | |||||
chr2:147930856
|
G | GT | 6 | a0001c0001t0014a0001c0001t0023a0001c0001t0035others(3): Show | 10 | HG02145.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4653dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4653 | chr2 | 147930856 | |||||
chr2:147930856
|
GT | G | 28 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(25): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*4653delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4653 | chr2 | 147930856 | |||||
chr2:147930878
|
T | A | 6 | a0001c0001t0018a0001c0001t0046a0001c0001t0048others(3): Show | 7 | HG02257.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4632A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4632 | chr2 | 147930878 | |||||
chr2:147930934
|
C | T | 1 | a0001c0001t0044 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4576G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4576 | chr2 | 147930934 | |||||
chr2:147930988
|
T | C | 3 | a0002c0002t0013a0002c0002t0015a0002c0002t0030 | 8 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4522A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4522 | chr2 | 147930988 | |||||
chr2:147930989
|
A | G | 2 | a0002c0002t0013a0002c0002t0015 | 7 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4521T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4521 | chr2 | 147930989 | |||||
chr2:147931006
|
A | AC | 5 | a0001c0001t0006a0001c0001t0018a0001c0001t0022others(2): Show | 12 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4503_*4504insG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4503 | chr2 | 147931006 | |||||
chr2:147931006
|
A | ACC | 5 | a0001c0001t0046a0001c0001t0047a0001c0001t0048others(2): Show | 5 | HG02818.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4503_*4504insGG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4503 | chr2 | 147931006 | |||||
chr2:147931006
|
A | C | 3 | a0002c0002t0013a0002c0002t0015a0002c0002t0030 | 8 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4504T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4504 | chr2 | 147931006 | |||||
chr2:147931007
|
T | C | 17 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(14): Show | 33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4503A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4503 | chr2 | 147931007 | |||||
chr2:147931021
|
A | C | 3 | a0002c0002t0013a0002c0002t0015a0002c0002t0030 | 8 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4489T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4489 | chr2 | 147931021 | |||||
chr2:147931077
|
A | G | 3 | a0001c0001t0014a0001c0001t0035a0001c0001t0057 | 6 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4433T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4433 | chr2 | 147931077 | |||||
chr2:147931125
|
T | C | 1 | a0001c0001t0012 | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4385A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4385 | chr2 | 147931125 | |||||
chr2:147931154
|
A | G | 1 | a0001c0001t0062 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4356T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4356 | chr2 | 147931154 | |||||
chr2:147931234
|
G | A | 2 | a0002c0002t0017a0002c0002t0027 | 3 | NA18942.hp2 NA18945.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4276C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 4276 | chr2 | 147931234 | |||||
chr2:147931520
|
T | C | 1 | a0001c0001t0026 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3990A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3990 | chr2 | 147931520 | |||||
chr2:147931537
|
A | ATGAT | 1 | a0002c0002t0015 | 3 | HG00140.hp1 HG01884.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3969_*3972dupATCA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3972 | chr2 | 147931537 | |||||
chr2:147931577
|
A | G | 1 | a0002c0002t0029 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3933T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3933 | chr2 | 147931577 | |||||
chr2:147931642
|
C | T | 1 | a0001c0001t0043 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3868G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3868 | chr2 | 147931642 | |||||
chr2:147931655
|
C | T | 1 | a0002c0002t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3855G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3855 | chr2 | 147931655 | |||||
chr2:147931678
|
G | A | 1 | a0002c0002t0032 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3832C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3832 | chr2 | 147931678 | |||||
chr2:147931708
|
C | T | 1 | a0001c0001t0019 | 2 | HG02615.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3802G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3802 | chr2 | 147931708 | |||||
chr2:147931756
|
A | G | 1 | a0001c0001t0056 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3754T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3754 | chr2 | 147931756 | |||||
chr2:147931789
|
G | T | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3721C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3721 | chr2 | 147931789 | |||||
chr2:147931800
|
T | C | 23 | a0001c0001t0012a0001c0001t0016a0001c0001t0026others(20): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3710A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3710 | chr2 | 147931800 | |||||
chr2:147931896
|
C | G | 28 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(25): Show | 87 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3614G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3614 | chr2 | 147931896 | |||||
chr2:147931917
|
C | T | 1 | a0001c0001t0046 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3593 | chr2 | 147931917 | |||||
chr2:147931935
|
T | TAA | 4 | a0001c0001t0014a0001c0001t0035a0001c0001t0056others(1): Show | 7 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3574_*3575insTT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3574 | chr2 | 147931935 | |||||
chr2:147931948
|
T | C | 21 | a0001c0001t0016a0002c0002t0002a0002c0002t0004others(18): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*3562A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3562 | chr2 | 147931948 | |||||
chr2:147931950
|
T | C | 1 | a0002c0002t0033 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3560A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3560 | chr2 | 147931950 | |||||
chr2:147931963
|
T | C | 1 | a0003c0003t0020 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3547A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3547 | chr2 | 147931963 | |||||
chr2:147932023
|
T | C | 1 | a0002c0002t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3487A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3487 | chr2 | 147932023 | |||||
chr2:147932035
|
T | C | 1 | a0001c0001t0045 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3475A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3475 | chr2 | 147932035 | |||||
chr2:147932151
|
T | C | 1 | a0002c0002t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3359A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3359 | chr2 | 147932151 | |||||
chr2:147932159
|
C | T | 13 | a0001c0001t0016a0002c0002t0002a0002c0002t0009others(10): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3351G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3351 | chr2 | 147932159 | |||||
chr2:147932189
|
T | G | 1 | a0001c0001t0026 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3321A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3321 | chr2 | 147932189 | |||||
chr2:147932202
|
A | G | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3308T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3308 | chr2 | 147932202 | |||||
chr2:147932282
|
G | A | 1 | a0001c0001t0021 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3228C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3228 | chr2 | 147932282 | |||||
chr2:147932284
|
T | C | 1 | a0001c0001t0021 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3226A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3226 | chr2 | 147932284 | |||||
chr2:147932442
|
T | C | 1 | a0001c0001t0012 | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3068A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3068 | chr2 | 147932442 | |||||
chr2:147932486
|
A | G | 23 | a0001c0001t0012a0001c0001t0016a0001c0001t0026others(20): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3024T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 3024 | chr2 | 147932486 | |||||
chr2:147932844
|
G | A | 6 | a0001c0001t0008a0001c0001t0022a0001c0001t0024others(3): Show | 13 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2666C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2666 | chr2 | 147932844 | |||||
chr2:147932869
|
A | ACT | 2 | a0001c0001t0012a0001c0001t0026 | 5 | HG00408.hp1 HG03516.hp1 NA18959.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2639_*2640dupAG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2640 | chr2 | 147932869 | |||||
chr2:147932994
|
A | T | 1 | a0001c0001t0061 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2516T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2516 | chr2 | 147932994 | |||||
chr2:147933026
|
A | AATC | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2481_*2483dupGAT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2483 | chr2 | 147933026 | |||||
chr2:147933258
|
G | A | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2252 | chr2 | 147933258 | |||||
chr2:147933261
|
T | G | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 2249 | chr2 | 147933261 | |||||
chr2:147933546
|
G | C | 1 | a0001c0001t0059 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1964 | chr2 | 147933546 | |||||
chr2:147933588
|
C | T | 1 | a0001c0001t0042 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1922 | chr2 | 147933588 | |||||
chr2:147933687
|
A | G | 6 | a0001c0001t0003a0001c0001t0028a0001c0001t0043others(3): Show | 41 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1823T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1823 | chr2 | 147933687 | |||||
chr2:147933776
|
G | A | 1 | a0001c0001t0012 | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1734C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1734 | chr2 | 147933776 | |||||
chr2:147933791
|
A | C | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1719T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1719 | chr2 | 147933791 | |||||
chr2:147933866
|
A | C | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1644 | chr2 | 147933866 | |||||
chr2:147933954
|
A | C | 1 | a0002c0002t0027 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1556 | chr2 | 147933954 | |||||
chr2:147934193
|
G | T | 1 | a0002c0002t0039 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1317 | chr2 | 147934193 | |||||
chr2:147934492
|
A | C | 1 | a0001c0001t0042 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 1018 | chr2 | 147934492 | |||||
chr2:147934558
|
T | G | 1 | a0001c0001t0060 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 952 | chr2 | 147934558 | |||||
chr2:147934664
|
A | G | 2 | a0001c0001t0012a0001c0001t0026 | 5 | HG00408.hp1 HG03516.hp1 NA18959.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 846 | chr2 | 147934664 | |||||
chr2:147934828
|
G | A | 1 | a0005c0006t0037 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 682 | chr2 | 147934828 | |||||
chr2:147935095
|
C | T | 1 | a0002c0002t0025 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 415 | chr2 | 147935095 | |||||
chr2:147935207
|
T | C | 7 | a0001c0001t0001a0001c0001t0023a0001c0001t0024others(4): Show | 87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*303A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 303 | chr2 | 147935207 | |||||
chr2:147935235
|
A | G | 1 | a0001c0001t0041 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 14/14 | 275 | chr2 | 147935235 | |||||
chr2:148020685
|
G | A | 1 | a0002c0002t0039 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/14 | 44727 | chr2 | 148020685 | |||||
chr2:148020698
|
G | A | 1 | a0002c0002t0040 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/14 | 44740 | chr2 | 148020698 | |||||
chr2:148020703
|
A | G | 24 | a0001c0001t0012a0001c0001t0026a0001c0001t0028others(21): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-88T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/14 | 44745 | chr2 | 148020703 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:147935712
|
G | T | 2 | a0001c0001t0014g0160a0001c0001t0014g0161 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1123-14C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147935712 | ||||||
chr2:147935955
|
A | G | 1 | a0001c0001t0008g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1123-257T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147935955 | ||||||
chr2:147936231
|
A | G | 1 | a0002c0002t0002g0006 | 2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1123-533T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936231 | ||||||
chr2:147936420
|
GA | G | 5 | a0001c0001t0001g0218a0001c0001t0001g0240a0001c0001t0003g0272others(2): Show | 5 | HG03139.hp1 HG03654.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-723delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936420 | ||||||
chr2:147936430
|
A | C | 1 | a0002c0002t0002g0104 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1123-732T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936430 | ||||||
chr2:147936747
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1123-1049C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936747 | ||||||
chr2:147936786
|
C | T | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1123-1088G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147936786 | ||||||
chr2:147937018
|
C | CA | 101 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0003g0281others(98): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1122+1127dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937018 | ||||||
chr2:147937018
|
C | CAA | 13 | a0001c0001t0001g0210a0001c0001t0008g0253a0001c0001t0012g0020others(10): Show | 13 | HG00408.hp1 HG00642.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1122+1126_1122+112 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937018 | ||||||
chr2:147937018
|
CA | C | 17 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0209others(14): Show | 18 | HG00738.hp1 HG01167.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1122+1127delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937018 | ||||||
chr2:147937283
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1122+863G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937283 | ||||||
chr2:147937490
|
A | G | 2 | a0002c0002t0002g0133a0002c0002t0031g0066 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1122+656T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937490 | ||||||
chr2:147937557
|
T | G | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1122+589A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937557 | ||||||
chr2:147937563
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+583A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937563 | ||||||
chr2:147937619
|
T | C | 3 | a0002c0002t0002g0107a0002c0002t0002g0120a0002c0002t0002g0121 | 3 | HG00544.hp1 NA18612.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1122+527A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937619 | ||||||
chr2:147937774
|
A | G | 3 | a0002c0002t0002g0001a0002c0002t0002g0097a0002c0002t0002g0119 | 5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122+372T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937774 | ||||||
chr2:147937972
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+174C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 13/13 | chr2 | 147937972 | ||||||
chr2:147938952
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+188G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 11/13 | chr2 | 147938952 | ||||||
chr2:147938991
|
C | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0203 | 2 | HG01081.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.958+149G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 11/13 | chr2 | 147938991 | ||||||
chr2:147939533
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.850-285T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939533 | ||||||
chr2:147939825
|
C | T | 1 | a0001c0001t0045g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.850-577G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939825 | ||||||
chr2:147939827
|
C | G | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-579G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939827 | ||||||
chr2:147939882
|
A | G | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-634T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939882 | ||||||
chr2:147939897
|
G | A | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.850-649C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939897 | ||||||
chr2:147939978
|
A | C | 1 | a0001c0001t0012g0022 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.850-730T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147939978 | ||||||
chr2:147940024
|
C | T | 20 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0026others(17): Show | 21 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-776G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940024 | ||||||
chr2:147940319
|
T | C | 5 | a0001c0001t0003g0282a0001c0001t0003g0285a0001c0001t0003g0286others(2): Show | 5 | HG00609.hp1 HG00673.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1071A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940319 | ||||||
chr2:147940630
|
G | GAT | 14 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0161others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.850-1384_850-1383d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940630 | ||||||
chr2:147940775
|
G | A | 5 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(2): Show | 5 | HG00408.hp1 HG03516.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1527C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940775 | ||||||
chr2:147940847
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.850-1599A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147940847 | ||||||
chr2:147941185
|
T | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0227others(1): Show | 4 | HG00558.hp1 NA18981.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-1937A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941185 | ||||||
chr2:147941241
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850-1993A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941241 | ||||||
chr2:147941310
|
T | C | 5 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0257others(2): Show | 5 | HG01167.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-2062A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941310 | ||||||
chr2:147941646
|
A | G | 1 | a0001c0001t0023g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.849+1790T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941646 | ||||||
chr2:147941661
|
T | A | 1 | a0002c0002t0004g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.849+1775A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941661 | ||||||
chr2:147941680
|
G | A | 1 | a0002c0002t0002g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.849+1756C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941680 | ||||||
chr2:147941772
|
G | GTA | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+1662_849+1663d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941772 | ||||||
chr2:147941895
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+1541T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147941895 | ||||||
chr2:147942323
|
A | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+1113T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942323 | ||||||
chr2:147942474
|
A | G | 1 | a0002c0002t0009g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.849+962T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942474 | ||||||
chr2:147942696
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+740A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942696 | ||||||
chr2:147942919
|
A | G | 2 | a0001c0001t0003g0292a0001c0001t0003g0293 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.849+517T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942919 | ||||||
chr2:147942969
|
G | T | 1 | a0002c0002t0002g0080 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.849+467C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147942969 | ||||||
chr2:147943079
|
G | C | 1 | a0002c0002t0002g0093 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.849+357C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943079 | ||||||
chr2:147943096
|
T | TGAAAGTA others(3309): Show |
1 | a0002c0002t0002g0135 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.849+339_849+340ins others(3316): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943096 | ||||||
chr2:147943346
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+90A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943346 | ||||||
chr2:147943376
|
C | A | 21 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0026others(18): Show | 22 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.849+60G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 10/13 | chr2 | 147943376 | ||||||
chr2:147943530
|
GA | G | 168 | a0001c0001t0001g0157a0001c0001t0001g0212a0001c0001t0006g0014others(165): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.763-9delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147943530 | ||||||
chr2:147943650
|
G | C | 1 | a0002c0002t0002g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.763-128C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147943650 | ||||||
chr2:147943852
|
T | C | 2 | a0002c0002t0002g0001a0002c0002t0002g0119 | 4 | NA18952.hp2 NA18962.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-330A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147943852 | ||||||
chr2:147944075
|
G | T | 1 | a0002c0002t0009g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.763-553C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944075 | ||||||
chr2:147944227
|
C | G | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(312): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.763-705G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944227 | ||||||
chr2:147944617
|
A | G | 1 | a0001c0001t0019g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.763-1095T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944617 | ||||||
chr2:147944661
|
T | C | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.763-1139A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944661 | ||||||
chr2:147944693
|
CT | C | 121 | a0001c0001t0003g0277a0001c0001t0026g0018a0002c0002t0002g0001others(118): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.763-1172delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944693 | ||||||
chr2:147944697
|
T | A | 5 | a0002c0002t0002g0122a0002c0002t0002g0133a0002c0002t0004g0029others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-1175A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944697 | ||||||
chr2:147944697
|
TA | T | 87 | a0001c0001t0001g0184a0001c0001t0001g0211a0001c0001t0003g0017others(84): Show | 91 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.763-1176delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944697 | ||||||
chr2:147944770
|
G | A | 2 | a0001c0001t0005g0214a0001c0001t0005g0230 | 2 | HG00738.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.763-1248C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147944770 | ||||||
chr2:147945426
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.763-1904A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945426 | ||||||
chr2:147945430
|
A | G | 128 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(125): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.763-1908T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945430 | ||||||
chr2:147945595
|
T | C | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.763-2073A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945595 | ||||||
chr2:147945643
|
A | G | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.763-2121T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945643 | ||||||
chr2:147945647
|
G | A | 1 | a0001c0001t0049g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.763-2125C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945647 | ||||||
chr2:147945741
|
C | T | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.763-2219G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945741 | ||||||
chr2:147945887
|
G | C | 2 | a0001c0001t0005g0176a0001c0001t0054g0175 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.762+2164C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147945887 | ||||||
chr2:147946293
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1758A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946293 | ||||||
chr2:147946295
|
G | GA | 38 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(35): Show | 39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.762+1755dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946295 | ||||||
chr2:147946377
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.762+1674T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946377 | ||||||
chr2:147946396
|
A | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(78): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.762+1655T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147946396 | ||||||
chr2:147947047
|
C | T | 38 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(35): Show | 41 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.762+1004G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947047 | ||||||
chr2:147947069
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.762+982G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947069 | ||||||
chr2:147947152
|
A | C | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.762+899T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947152 | ||||||
chr2:147947164
|
T | C | 3 | a0001c0001t0005g0176a0001c0001t0054g0175a0005c0006t0037g0047 | 3 | HG02280.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.762+887A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947164 | ||||||
chr2:147947280
|
G | A | 1 | a0001c0001t0014g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.762+771C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947280 | ||||||
chr2:147947337
|
C | A | 1 | a0001c0001t0005g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.762+714G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947337 | ||||||
chr2:147947363
|
T | C | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.762+688A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947363 | ||||||
chr2:147947410
|
C | T | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.762+641G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947410 | ||||||
chr2:147947502
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0198 | 3 | HG02071.hp2 NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.762+549T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947502 | ||||||
chr2:147947564
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.762+487C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947564 | ||||||
chr2:147947784
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+267G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947784 | ||||||
chr2:147947855
|
G | C | 1 | a0001c0001t0003g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.762+196C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 9/13 | chr2 | 147947855 | ||||||
chr2:147948349
|
A | G | 1 | a0003c0003t0011g0235 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.589-125T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948349 | ||||||
chr2:147948653
|
C | T | 1 | a0001c0001t0003g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.589-429G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948653 | ||||||
chr2:147948670
|
C | CT | 6 | a0001c0001t0001g0201a0001c0001t0003g0292a0001c0001t0003g0293others(3): Show | 6 | HG00673.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-447dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948670 | ||||||
chr2:147948801
|
G | T | 88 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(85): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.589-577C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948801 | ||||||
chr2:147948928
|
C | T | 214 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(211): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.589-704G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948928 | ||||||
chr2:147948995
|
G | GCATATTA others(18): Show |
1 | a0001c0001t0045g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.589-796_589-772dup others(25): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147948995 | ||||||
chr2:147949005
|
T | G | 1 | a0003c0003t0011g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.589-781A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949005 | ||||||
chr2:147949024
|
A | G | 25 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0026others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.589-800T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949024 | ||||||
chr2:147949054
|
T | C | 1 | a0001c0001t0056g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.589-830A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949054 | ||||||
chr2:147949197
|
A | G | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-973T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949197 | ||||||
chr2:147949463
|
C | T | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.589-1239G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949463 | ||||||
chr2:147949950
|
C | G | 7 | a0001c0001t0003g0166a0001c0001t0014g0159a0001c0001t0014g0160others(4): Show | 7 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-1726G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949950 | ||||||
chr2:147949950
|
C | T | 11 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0026others(8): Show | 12 | HG00738.hp2 HG01175.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-1726G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949950 | ||||||
chr2:147949968
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589-1744A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147949968 | ||||||
chr2:147950156
|
A | G | 1 | a0001c0001t0008g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.589-1932T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950156 | ||||||
chr2:147950253
|
C | T | 1 | a0002c0002t0002g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.589-2029G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950253 | ||||||
chr2:147950262
|
G | T | 3 | a0001c0001t0001g0202a0002c0002t0004g0029a0002c0002t0004g0030 | 3 | HG02895.hp2 HG03139.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.589-2038C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950262 | ||||||
chr2:147950397
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.588+1976T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950397 | ||||||
chr2:147950541
|
T | C | 46 | a0001c0001t0001g0242a0001c0001t0012g0020a0001c0001t0012g0021others(43): Show | 48 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.588+1832A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950541 | ||||||
chr2:147950563
|
G | C | 2 | a0002c0002t0002g0133a0002c0002t0031g0066 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.588+1810C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950563 | ||||||
chr2:147950564
|
A | G | 2 | a0001c0001t0021g0187a0001c0001t0021g0306 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.588+1809T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950564 | ||||||
chr2:147950764
|
C | CA | 159 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(156): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.588+1608dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950764 | ||||||
chr2:147950939
|
G | A | 1 | a0003c0003t0011g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.588+1434C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950939 | ||||||
chr2:147950943
|
A | AT | 87 | a0001c0001t0060g0294a0002c0002t0002g0001a0002c0002t0002g0006others(84): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.588+1429dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950943 | ||||||
chr2:147950993
|
G | A | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.588+1380C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147950993 | ||||||
chr2:147951088
|
T | C | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.588+1285A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951088 | ||||||
chr2:147951277
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.588+1096G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951277 | ||||||
chr2:147951310
|
T | G | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.588+1063A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951310 | ||||||
chr2:147951547
|
G | A | 5 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(2): Show | 6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+826C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951547 | ||||||
chr2:147951583
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.588+790A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951583 | ||||||
chr2:147951615
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.588+758C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951615 | ||||||
chr2:147951801
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG00544.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.588+572G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147951801 | ||||||
chr2:147952084
|
A | G | 88 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(85): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.588+289T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147952084 | ||||||
chr2:147952201
|
C | T | 1 | a0001c0001t0041g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.588+172G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 8/13 | chr2 | 147952201 | ||||||
chr2:147952722
|
C | T | 5 | a0001c0001t0003g0273a0001c0001t0003g0295a0001c0001t0003g0312others(2): Show | 5 | NA18943.hp1 NA18985.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-198G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147952722 | ||||||
chr2:147952792
|
T | C | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.437-268A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147952792 | ||||||
chr2:147952941
|
G | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-417C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147952941 | ||||||
chr2:147953159
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0168a0001c0001t0001g0201others(2): Show | 6 | NA18960.hp2 NA18980.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-635T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953159 | ||||||
chr2:147953170
|
TA | T | 78 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(75): Show | 80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.437-647delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953170 | ||||||
chr2:147953237
|
A | G | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.437-713T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953237 | ||||||
chr2:147953275
|
A | G | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-751T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953275 | ||||||
chr2:147953403
|
A | G | 1 | a0002c0002t0002g0086 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.437-879T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953403 | ||||||
chr2:147953606
|
G | T | 214 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(211): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.437-1082C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147953606 | ||||||
chr2:147954015
|
G | T | 4 | a0002c0002t0002g0051a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1332C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954015 | ||||||
chr2:147954122
|
A | C | 1 | a0002c0002t0029g0138 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.436+1225T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954122 | ||||||
chr2:147954512
|
C | A | 21 | a0001c0001t0006g0016a0001c0001t0008g0249a0001c0001t0008g0252others(18): Show | 22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.436+835G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954512 | ||||||
chr2:147954614
|
T | C | 1 | a0002c0002t0013g0136 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.436+733A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954614 | ||||||
chr2:147954667
|
A | G | 1 | a0002c0002t0002g0108 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.436+680T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954667 | ||||||
chr2:147954844
|
T | A | 1 | a0001c0001t0003g0291 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.436+503A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147954844 | ||||||
chr2:147955250
|
CT | C | 23 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0026others(20): Show | 24 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.436+96delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 7/13 | chr2 | 147955250 | ||||||
chr2:147955547
|
A | G | 1 | a0002c0002t0013g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.388-152T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955547 | ||||||
chr2:147955689
|
G | A | 4 | a0002c0002t0002g0010a0002c0002t0002g0114a0002c0002t0002g0115others(1): Show | 5 | HG01123.hp2 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-294C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955689 | ||||||
chr2:147955899
|
T | C | 1 | a0001c0001t0001g0011 | 2 | NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.388-504A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955899 | ||||||
chr2:147955919
|
C | T | 2 | a0002c0002t0002g0133a0002c0002t0031g0066 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.388-524G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955919 | ||||||
chr2:147955930
|
T | C | 1 | a0001c0001t0041g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.388-535A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955930 | ||||||
chr2:147955983
|
C | A | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388-588G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955983 | ||||||
chr2:147955984
|
C | A | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388-589G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147955984 | ||||||
chr2:147956038
|
G | T | 39 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.388-643C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956038 | ||||||
chr2:147956085
|
T | C | 10 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0253others(7): Show | 10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.388-690A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956085 | ||||||
chr2:147956097
|
A | T | 2 | a0001c0001t0003g0292a0001c0001t0003g0293 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.388-702T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956097 | ||||||
chr2:147956268
|
T | C | 1 | a0002c0002t0002g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.388-873A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956268 | ||||||
chr2:147956555
|
A | T | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.388-1160T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956555 | ||||||
chr2:147956748
|
C | T | 1 | a0001c0004t0006g0266 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.388-1353G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956748 | ||||||
chr2:147956810
|
T | C | 1 | a0002c0002t0002g0056 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.388-1415A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956810 | ||||||
chr2:147956825
|
A | G | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388-1430T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956825 | ||||||
chr2:147956833
|
A | T | 1 | a0002c0002t0002g0064 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.388-1438T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147956833 | ||||||
chr2:147957156
|
T | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0209others(1): Show | 4 | HG01256.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1142A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957156 | ||||||
chr2:147957348
|
T | G | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.387+950A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957348 | ||||||
chr2:147957469
|
T | C | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.387+829A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957469 | ||||||
chr2:147957677
|
G | A | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.387+621C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957677 | ||||||
chr2:147957787
|
C | T | 1 | a0002c0002t0002g0019 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.387+511G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147957787 | ||||||
chr2:147958025
|
T | C | 1 | a0001c0001t0003g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.387+273A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147958025 | ||||||
chr2:147958219
|
C | T | 1 | a0002c0002t0013g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.387+79G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 6/13 | chr2 | 147958219 | ||||||
chr2:147958406
|
G | T | 1 | a0002c0002t0002g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.302-23C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958406 | ||||||
chr2:147958482
|
T | A | 5 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(2): Show | 6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-99A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958482 | ||||||
chr2:147958530
|
G | T | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.302-147C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958530 | ||||||
chr2:147958595
|
A | C | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.301+196T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 5/13 | chr2 | 147958595 | ||||||
chr2:147958877
|
A | C | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.226-11T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147958877 | ||||||
chr2:147959141
|
T | G | 21 | a0002c0002t0002g0007a0002c0002t0002g0071a0002c0002t0002g0072others(18): Show | 22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.226-275A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959141 | ||||||
chr2:147959242
|
T | C | 1 | a0001c0001t0050g0244 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.226-376A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959242 | ||||||
chr2:147959260
|
C | G | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-394G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959260 | ||||||
chr2:147959261
|
C | T | 214 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(211): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.226-395G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959261 | ||||||
chr2:147959361
|
C | CT | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-496dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959361 | ||||||
chr2:147959621
|
A | G | 1 | a0002c0002t0004g0035 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.226-755T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959621 | ||||||
chr2:147959911
|
G | A | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-1045C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959911 | ||||||
chr2:147959928
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-1062A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147959928 | ||||||
chr2:147960038
|
C | T | 26 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0026others(23): Show | 27 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.226-1172G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960038 | ||||||
chr2:147960289
|
A | G | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1423T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960289 | ||||||
chr2:147960583
|
C | T | 1 | a0002c0002t0002g0055 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.226-1717G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960583 | ||||||
chr2:147960617
|
C | CTA | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.226-1752_226-1751i others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960617 | ||||||
chr2:147960849
|
G | A | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1983C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960849 | ||||||
chr2:147960914
|
T | A | 1 | a0002c0002t0002g0111 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.226-2048A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960914 | ||||||
chr2:147960950
|
T | A | 1 | a0002c0002t0004g0024 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226-2084A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147960950 | ||||||
chr2:147961118
|
T | C | 6 | a0002c0002t0002g0006a0002c0002t0002g0062a0002c0002t0002g0063others(3): Show | 7 | HG02083.hp1 NA18948.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-2252A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961118 | ||||||
chr2:147961351
|
T | C | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.226-2485A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961351 | ||||||
chr2:147961438
|
GA | G | 168 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(165): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.226-2573delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961438 | ||||||
chr2:147961820
|
C | T | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.226-2954G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961820 | ||||||
chr2:147961844
|
T | C | 1 | a0001c0001t0007g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-2978A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147961844 | ||||||
chr2:147962235
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.226-3369T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962235 | ||||||
chr2:147962534
|
C | T | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-3668G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962534 | ||||||
chr2:147962618
|
A | G | 206 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.226-3752T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962618 | ||||||
chr2:147962704
|
C | G | 1 | a0002c0002t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.226-3838G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962704 | ||||||
chr2:147962747
|
G | A | 4 | a0001c0001t0001g0210a0002c0002t0002g0101a0002c0002t0002g0102others(1): Show | 4 | HG01981.hp1 NA18969.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-3881C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962747 | ||||||
chr2:147962778
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-3912G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962778 | ||||||
chr2:147962869
|
G | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-4003C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962869 | ||||||
chr2:147962984
|
G | T | 1 | a0001c0001t0054g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226-4118C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147962984 | ||||||
chr2:147963019
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4153G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963019 | ||||||
chr2:147963100
|
C | A | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-4234G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963100 | ||||||
chr2:147963155
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4289G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963155 | ||||||
chr2:147963276
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4410A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963276 | ||||||
chr2:147963362
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.226-4496C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963362 | ||||||
chr2:147963460
|
T | A | 1 | a0002c0002t0002g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.226-4594A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963460 | ||||||
chr2:147963465
|
A | G | 1 | a0002c0002t0004g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.226-4599T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963465 | ||||||
chr2:147963537
|
A | G | 2 | a0001c0001t0024g0191a0001c0001t0024g0192 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.226-4671T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963537 | ||||||
chr2:147963734
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-4868A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963734 | ||||||
chr2:147963888
|
T | C | 1 | a0001c0001t0012g0022 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.226-5022A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963888 | ||||||
chr2:147963897
|
C | A | 2 | a0001c0001t0003g0288a0001c0001t0003g0289 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.226-5031G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147963897 | ||||||
chr2:147964165
|
G | A | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-5299C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964165 | ||||||
chr2:147964254
|
A | G | 3 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0232 | 3 | HG00642.hp2 HG00741.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.226-5388T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964254 | ||||||
chr2:147964301
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.226-5435A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964301 | ||||||
chr2:147964415
|
T | A | 1 | a0001c0001t0046g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-5549A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964415 | ||||||
chr2:147964714
|
C | T | 39 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.226-5848G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964714 | ||||||
chr2:147964863
|
C | T | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226-5997G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964863 | ||||||
chr2:147964875
|
T | C | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226-6009A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964875 | ||||||
chr2:147964905
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-6039C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964905 | ||||||
chr2:147964956
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.226-6090T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147964956 | ||||||
chr2:147965037
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-6171G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965037 | ||||||
chr2:147965308
|
T | C | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-6442A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965308 | ||||||
chr2:147965557
|
A | C | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-6691T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965557 | ||||||
chr2:147965596
|
A | G | 30 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(27): Show | 33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.226-6730T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965596 | ||||||
chr2:147965757
|
G | A | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226-6891C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965757 | ||||||
chr2:147965948
|
G | A | 2 | a0002c0002t0002g0081a0002c0002t0002g0082 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.225+6791C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147965948 | ||||||
chr2:147966049
|
T | A | 1 | a0002c0002t0002g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225+6690A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966049 | ||||||
chr2:147966050
|
A | T | 3 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022 | 3 | HG00408.hp1 NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.225+6689T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966050 | ||||||
chr2:147966071
|
GAACATTA others(13): Show |
G | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225+6648_225+6667d others(22): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966071 | ||||||
chr2:147966340
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.225+6399T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966340 | ||||||
chr2:147966343
|
T | C | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+6396A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966343 | ||||||
chr2:147966600
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.225+6139G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966600 | ||||||
chr2:147966696
|
G | A | 1 | a0002c0002t0004g0033 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.225+6043C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966696 | ||||||
chr2:147966787
|
T | C | 1 | a0001c0001t0003g0285 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.225+5952A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966787 | ||||||
chr2:147966845
|
G | A | 2 | a0002c0002t0002g0102a0002c0002t0002g0111 | 2 | NA18969.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.225+5894C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966845 | ||||||
chr2:147966988
|
A | G | 39 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.225+5751T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966988 | ||||||
chr2:147966992
|
T | C | 1 | a0002c0002t0040g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.225+5747A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147966992 | ||||||
chr2:147967102
|
T | C | 39 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.225+5637A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967102 | ||||||
chr2:147967288
|
C | T | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225+5451G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967288 | ||||||
chr2:147967449
|
C | T | 8 | a0001c0001t0041g0234a0003c0003t0011g0143a0003c0003t0011g0233others(5): Show | 8 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+5290G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967449 | ||||||
chr2:147967559
|
G | A | 1 | a0002c0002t0032g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.225+5180C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967559 | ||||||
chr2:147967591
|
G | A | 1 | a0001c0001t0045g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.225+5148C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967591 | ||||||
chr2:147967595
|
A | G | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+5144T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967595 | ||||||
chr2:147967997
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.225+4742T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147967997 | ||||||
chr2:147968002
|
C | T | 1 | a0001c0001t0006g0014 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225+4737G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968002 | ||||||
chr2:147968171
|
G | C | 7 | a0001c0001t0003g0273a0001c0001t0003g0295a0001c0001t0003g0296others(4): Show | 7 | NA18943.hp1 NA18948.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+4568C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968171 | ||||||
chr2:147968376
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225+4363A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968376 | ||||||
chr2:147968680
|
T | C | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+4059A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147968680 | ||||||
chr2:147969021
|
T | C | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.225+3718A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969021 | ||||||
chr2:147969052
|
G | A | 2 | a0001c0001t0019g0301a0001c0001t0019g0302 | 2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.225+3687C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969052 | ||||||
chr2:147969202
|
A | T | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.225+3537T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969202 | ||||||
chr2:147969257
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.225+3482T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969257 | ||||||
chr2:147969406
|
T | A | 1 | a0001c0001t0050g0244 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.225+3333A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969406 | ||||||
chr2:147969457
|
C | T | 214 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(211): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.225+3282G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969457 | ||||||
chr2:147969922
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225+2817A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147969922 | ||||||
chr2:147970154
|
CAT | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+2583_225+2584d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970154 | ||||||
chr2:147970194
|
A | G | 1 | a0005c0006t0037g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.225+2545T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970194 | ||||||
chr2:147970225
|
C | T | 5 | a0001c0001t0003g0292a0001c0001t0003g0293a0001c0001t0024g0191others(2): Show | 5 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+2514G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970225 | ||||||
chr2:147970293
|
A | T | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2446T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970293 | ||||||
chr2:147970423
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+2316A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970423 | ||||||
chr2:147970589
|
T | C | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.225+2150A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970589 | ||||||
chr2:147970593
|
T | C | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2146A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970593 | ||||||
chr2:147970615
|
C | CA | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.225+2123dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970615 | ||||||
chr2:147970627
|
A | G | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2112T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970627 | ||||||
chr2:147970628
|
G | A | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+2111C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970628 | ||||||
chr2:147970628
|
G | GA | 7 | a0001c0001t0001g0206a0001c0001t0003g0286a0001c0001t0005g0167others(4): Show | 7 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+2110dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970628 | ||||||
chr2:147970739
|
T | C | 1 | a0001c0001t0003g0290 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.225+2000A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970739 | ||||||
chr2:147970743
|
A | T | 7 | a0002c0002t0002g0099a0002c0002t0002g0103a0002c0002t0002g0104others(4): Show | 7 | HG00438.hp1 NA18943.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1996T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970743 | ||||||
chr2:147970871
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.225+1868T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147970871 | ||||||
chr2:147971272
|
AAT | A | 3 | a0001c0001t0003g0166a0001c0001t0035g0025a0001c0001t0057g0162 | 3 | HG01243.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.225+1465_225+1466d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971272 | ||||||
chr2:147971409
|
C | T | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225+1330G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971409 | ||||||
chr2:147971469
|
A | G | 1 | a0002c0002t0004g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.225+1270T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971469 | ||||||
chr2:147971481
|
T | C | 217 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(214): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.225+1258A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971481 | ||||||
chr2:147971528
|
T | C | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.225+1211A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971528 | ||||||
chr2:147971533
|
A | G | 1 | a0002c0002t0038g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225+1206T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971533 | ||||||
chr2:147971922
|
C | G | 37 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(34): Show | 38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.225+817G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971922 | ||||||
chr2:147971957
|
G | A | 1 | a0001c0001t0003g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.225+782C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971957 | ||||||
chr2:147971998
|
A | G | 2 | a0002c0002t0002g0108a0002c0002t0002g0109 | 2 | NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.225+741T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147971998 | ||||||
chr2:147972040
|
C | A | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+699G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972040 | ||||||
chr2:147972041
|
A | C | 1 | a0002c0002t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225+698T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972041 | ||||||
chr2:147972178
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.225+561A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972178 | ||||||
chr2:147972396
|
T | G | 2 | a0001c0001t0005g0167a0001c0001t0052g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.225+343A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972396 | ||||||
chr2:147972532
|
T | G | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+207A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 4/13 | chr2 | 147972532 | ||||||
chr2:147972885
|
T | C | 3 | a0002c0002t0002g0001a0002c0002t0002g0097a0002c0002t0002g0119 | 5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-56A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147972885 | ||||||
chr2:147973058
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.135-229A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973058 | ||||||
chr2:147973070
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.135-241G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973070 | ||||||
chr2:147973305
|
T | C | 1 | a0002c0002t0004g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.134+143A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973305 | ||||||
chr2:147973337
|
T | C | 2 | a0002c0002t0002g0108a0002c0002t0002g0109 | 2 | NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.134+111A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 3/13 | chr2 | 147973337 | ||||||
chr2:147973683
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(310): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.58-159A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973683 | ||||||
chr2:147973684
|
G | A | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.58-160C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973684 | ||||||
chr2:147973686
|
T | TA | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.58-163dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973686 | ||||||
chr2:147973762
|
G | A | 2 | a0002c0002t0002g0114a0002c0002t0002g0115 | 2 | HG01123.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.58-238C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973762 | ||||||
chr2:147973823
|
C | T | 1 | a0001c0001t0019g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-299G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973823 | ||||||
chr2:147973826
|
G | A | 1 | a0002c0002t0002g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58-302C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147973826 | ||||||
chr2:147974103
|
T | C | 1 | a0001c0001t0056g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-579A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974103 | ||||||
chr2:147974290
|
G | T | 213 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(210): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.58-766C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974290 | ||||||
chr2:147974372
|
G | A | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-848C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974372 | ||||||
chr2:147974381
|
C | T | 88 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(85): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.58-857G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974381 | ||||||
chr2:147974385
|
A | G | 1 | a0002c0002t0036g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-861T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974385 | ||||||
chr2:147974466
|
C | A | 8 | a0001c0001t0003g0166a0001c0001t0014g0159a0001c0001t0014g0160others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-942G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974466 | ||||||
chr2:147974530
|
G | C | 83 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(80): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.58-1006C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974530 | ||||||
chr2:147974591
|
C | T | 12 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0253others(9): Show | 12 | HG01167.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-1067G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974591 | ||||||
chr2:147974628
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58-1104A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974628 | ||||||
chr2:147974807
|
T | TA | 11 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0190others(8): Show | 11 | HG00099.hp1 HG00642.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+1094dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974807 | ||||||
chr2:147974807
|
TA | T | 132 | a0001c0001t0001g0169a0001c0001t0003g0017a0001c0001t0003g0166others(129): Show | 139 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.57+1094delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974807 | ||||||
chr2:147974841
|
T | C | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.57+1061A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974841 | ||||||
chr2:147974866
|
G | A | 25 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+1036C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147974866 | ||||||
chr2:147975010
|
T | A | 7 | a0001c0001t0003g0273a0001c0001t0003g0295a0001c0001t0003g0296others(4): Show | 7 | NA18943.hp1 NA18948.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+892A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975010 | ||||||
chr2:147975134
|
A | G | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.57+768T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975134 | ||||||
chr2:147975141
|
G | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0197a0001c0001t0001g0200others(1): Show | 4 | HG00609.hp2 NA18945.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+761C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975141 | ||||||
chr2:147975194
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+708G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975194 | ||||||
chr2:147975215
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+687C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975215 | ||||||
chr2:147975354
|
A | G | 1 | a0002c0002t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57+548T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975354 | ||||||
chr2:147975364
|
A | G | 1 | a0001c0001t0003g0273 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57+538T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975364 | ||||||
chr2:147975426
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.57+476A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975426 | ||||||
chr2:147975506
|
GA | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(175): Show | 189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.57+395delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975506 | ||||||
chr2:147975506
|
GAAA | G | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.57+393_57+395delTT others(1): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975506 | ||||||
chr2:147975624
|
T | A | 1 | a0002c0002t0009g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.57+278A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975624 | ||||||
chr2:147975750
|
C | T | 1 | a0002c0002t0038g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.57+152G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975750 | ||||||
chr2:147975784
|
T | C | 25 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+118A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 2/13 | chr2 | 147975784 | ||||||
chr2:147975979
|
T | TA | 222 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(219): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
splice_region_variant&intron_variant | LOW | c.-17-5dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147975979 | ||||||
chr2:147976230
|
G | A | 30 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(27): Show | 33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-255C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976230 | ||||||
chr2:147976291
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-17-316T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976291 | ||||||
chr2:147976475
|
G | T | 1 | a0002c0002t0004g0125 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17-500C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976475 | ||||||
chr2:147976659
|
G | C | 1 | a0001c0001t0003g0287 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-17-684C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976659 | ||||||
chr2:147976892
|
A | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0198 | 3 | HG02071.hp2 NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-17-917T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976892 | ||||||
chr2:147976912
|
TCTC | T | 39 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-940_-17-938del others(3): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147976912 | ||||||
chr2:147977084
|
C | T | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1109G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977084 | ||||||
chr2:147977106
|
T | C | 2 | a0001c0001t0003g0288a0001c0001t0003g0289 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-17-1131A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977106 | ||||||
chr2:147977120
|
T | C | 1 | a0001c0001t0003g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-1145A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977120 | ||||||
chr2:147977260
|
T | C | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-1285A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977260 | ||||||
chr2:147977324
|
G | C | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-1349C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977324 | ||||||
chr2:147977355
|
T | G | 1 | a0001c0001t0012g0022 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-17-1380A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977355 | ||||||
chr2:147977400
|
T | C | 1 | a0005c0006t0037g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-1425A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977400 | ||||||
chr2:147977680
|
T | TA | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-1706dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977680 | ||||||
chr2:147977819
|
G | C | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-17-1844C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977819 | ||||||
chr2:147977975
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-17-2000G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147977975 | ||||||
chr2:147978012
|
G | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-2037C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978012 | ||||||
chr2:147978105
|
C | T | 1 | a0002c0002t0010g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-2130G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978105 | ||||||
chr2:147978110
|
C | T | 1 | a0005c0006t0037g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-2135G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978110 | ||||||
chr2:147978243
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2268A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978243 | ||||||
chr2:147978434
|
A | G | 20 | a0001c0001t0003g0017a0001c0001t0003g0272a0001c0001t0003g0274others(17): Show | 21 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-2459T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978434 | ||||||
chr2:147978464
|
C | T | 1 | a0001c0001t0041g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-17-2489G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978464 | ||||||
chr2:147978553
|
C | T | 1 | a0001c0001t0019g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-17-2578G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978553 | ||||||
chr2:147978570
|
T | C | 1 | a0002c0002t0002g0063 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-17-2595A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978570 | ||||||
chr2:147978586
|
G | A | 3 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314 | 3 | NA18988.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-17-2611C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978586 | ||||||
chr2:147978669
|
G | A | 2 | a0001c0001t0003g0292a0001c0001t0003g0293 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-17-2694C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978669 | ||||||
chr2:147978796
|
C | T | 1 | a0001c0001t0061g0220 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-17-2821G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147978796 | ||||||
chr2:147979021
|
A | G | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-3046T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979021 | ||||||
chr2:147979038
|
C | T | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-3063G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979038 | ||||||
chr2:147979481
|
A | G | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-3506T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979481 | ||||||
chr2:147979484
|
A | G | 5 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0257others(2): Show | 5 | HG01167.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-3509T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979484 | ||||||
chr2:147979714
|
T | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0209others(4): Show | 7 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-3739A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979714 | ||||||
chr2:147979756
|
C | T | 119 | a0001c0001t0003g0284a0002c0002t0002g0001a0002c0002t0002g0006others(116): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-17-3781G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979756 | ||||||
chr2:147979790
|
TGTTCAAC others(4): Show |
T | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-3826_-17-3816d others(13): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979790 | ||||||
chr2:147979917
|
G | C | 8 | a0001c0001t0006g0014a0001c0001t0006g0243a0001c0001t0006g0246others(5): Show | 10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-3942C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979917 | ||||||
chr2:147979992
|
T | C | 1 | a0002c0002t0009g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-17-4017A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147979992 | ||||||
chr2:147980044
|
C | G | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-4069G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980044 | ||||||
chr2:147980260
|
T | A | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-17-4285A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980260 | ||||||
chr2:147980449
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-4474C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980449 | ||||||
chr2:147980616
|
C | T | 1 | a0002c0002t0009g0091 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-17-4641G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980616 | ||||||
chr2:147980958
|
A | C | 2 | a0002c0002t0002g0083a0002c0002t0002g0085 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17-4983T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980958 | ||||||
chr2:147980965
|
C | T | 1 | a0002c0002t0010g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-4990G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147980965 | ||||||
chr2:147981251
|
T | C | 1 | a0001c0001t0003g0290 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-17-5276A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981251 | ||||||
chr2:147981504
|
G | C | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-5529C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981504 | ||||||
chr2:147981546
|
T | C | 8 | a0002c0002t0002g0009a0002c0002t0002g0088a0002c0002t0002g0090others(5): Show | 9 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-5571A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981546 | ||||||
chr2:147981552
|
G | T | 2 | a0002c0002t0002g0068a0002c0002t0002g0069 | 2 | NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-17-5577C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981552 | ||||||
chr2:147981602
|
C | A | 1 | a0002c0002t0004g0037 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-5627G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981602 | ||||||
chr2:147981681
|
A | G | 2 | a0001c0004t0006g0266a0001c0004t0007g0268 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-17-5706T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981681 | ||||||
chr2:147981744
|
T | TG | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(312): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-17-5770dupC | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981744 | ||||||
chr2:147981824
|
G | A | 168 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(165): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-17-5849C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147981824 | ||||||
chr2:147982102
|
A | G | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-6127T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982102 | ||||||
chr2:147982160
|
C | A | 1 | a0002c0002t0002g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-17-6185G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982160 | ||||||
chr2:147982254
|
G | C | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17-6279C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982254 | ||||||
chr2:147982911
|
A | G | 1 | a0002c0002t0002g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-17-6936T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982911 | ||||||
chr2:147982912
|
T | C | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-6937A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982912 | ||||||
chr2:147982941
|
C | T | 5 | a0001c0001t0005g0167a0001c0001t0005g0307a0001c0001t0005g0308others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-6966G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147982941 | ||||||
chr2:147983018
|
C | T | 128 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(125): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-17-7043G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983018 | ||||||
chr2:147983264
|
C | T | 25 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17-7289G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983264 | ||||||
chr2:147983485
|
G | T | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-7510C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983485 | ||||||
chr2:147983673
|
A | C | 1 | a0001c0001t0008g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17-7698T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983673 | ||||||
chr2:147983834
|
C | G | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(312): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-17-7859G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147983834 | ||||||
chr2:147984052
|
C | T | 83 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(80): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-17-8077G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984052 | ||||||
chr2:147984091
|
A | G | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-8116T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984091 | ||||||
chr2:147984192
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-17-8217G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984192 | ||||||
chr2:147984205
|
C | T | 37 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(34): Show | 38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-8230G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984205 | ||||||
chr2:147984409
|
T | C | 124 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17-8434A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984409 | ||||||
chr2:147984411
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-17-8436G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984411 | ||||||
chr2:147984543
|
G | A | 7 | a0001c0001t0006g0014a0001c0001t0006g0243a0001c0001t0006g0246others(4): Show | 9 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-8568C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984543 | ||||||
chr2:147984608
|
C | T | 1 | a0001c0001t0045g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-17-8633G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984608 | ||||||
chr2:147984612
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-17-8637T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984612 | ||||||
chr2:147984745
|
C | A | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-8770G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984745 | ||||||
chr2:147984942
|
A | G | 1 | a0002c0002t0002g0098 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-17-8967T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147984942 | ||||||
chr2:147985035
|
T | G | 1 | a0001c0001t0003g0295 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-17-9060A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985035 | ||||||
chr2:147985263
|
C | G | 1 | a0001c0001t0003g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17-9288G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985263 | ||||||
chr2:147985266
|
G | A | 8 | a0001c0001t0006g0014a0001c0001t0006g0243a0001c0001t0006g0246others(5): Show | 10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-9291C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985266 | ||||||
chr2:147985271
|
A | G | 25 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17-9296T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985271 | ||||||
chr2:147985333
|
A | G | 10 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0253others(7): Show | 10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-9358T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985333 | ||||||
chr2:147985387
|
G | A | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-9412C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147985387 | ||||||
chr2:147986504
|
G | A | 8 | a0001c0001t0003g0166a0001c0001t0014g0159a0001c0001t0014g0160others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-10529C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986504 | ||||||
chr2:147986744
|
C | T | 8 | a0001c0001t0041g0234a0003c0003t0011g0143a0003c0003t0011g0233others(5): Show | 8 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-10769G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986744 | ||||||
chr2:147986790
|
T | C | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-10815A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TAC | 15 | a0001c0001t0001g0185a0001c0001t0001g0193a0001c0001t0001g0231others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-10817_-17-1081 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACAC | 70 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(67): Show | 73 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-17-10819_-17-1081 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACAC | 28 | a0001c0001t0003g0166a0001c0001t0003g0292a0001c0001t0003g0293others(25): Show | 28 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-10821_-17-1081 others(10): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACACA others(1): Show |
88 | a0001c0001t0006g0016a0001c0001t0012g0020a0001c0001t0012g0021others(85): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-10823_-17-1081 others(12): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACACA others(3): Show |
15 | a0001c0001t0018g0265a0001c0004t0006g0266a0002c0002t0002g0010others(12): Show | 16 | HG01168.hp2 HG01943.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-10825_-17-1081 others(14): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACACA others(5): Show |
2 | a0001c0001t0007g0248a0001c0001t0059g0158 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-17-10827_-17-1081 others(16): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACACA others(7): Show |
2 | a0001c0001t0007g0245a0001c0001t0050g0244 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-17-10829_-17-1081 others(18): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACACA others(9): Show |
4 | a0001c0001t0006g0243a0001c0001t0006g0246a0001c0001t0007g0015others(1): Show | 5 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-10831_-17-1081 others(20): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986790
|
T | TACACACA others(11): Show |
1 | a0001c0001t0006g0014 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-17-10833_-17-1081 others(22): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986790 | ||||||
chr2:147986814
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-17-10839G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147986814 | ||||||
chr2:147987186
|
T | TA | 121 | a0001c0001t0001g0144a0002c0002t0002g0001a0002c0002t0002g0006others(118): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-17-11212dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987186 | ||||||
chr2:147987273
|
T | TAC | 6 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0002g0068others(3): Show | 6 | NA18944.hp1 NA18986.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-11300_-17-1129 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987273 | ||||||
chr2:147987289
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-11314A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987289 | ||||||
chr2:147987357
|
G | GAT | 4 | a0002c0002t0013g0060a0002c0002t0015g0076a0002c0002t0015g0077others(1): Show | 4 | HG00140.hp1 HG01884.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-11384_-17-1138 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987357 | ||||||
chr2:147987366
|
A | ATATG | 119 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(116): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-17-11392_-17-1139 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987366 | ||||||
chr2:147987366
|
A | ATG | 96 | a0001c0001t0001g0311a0001c0001t0003g0017a0001c0001t0003g0269others(93): Show | 100 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-17-11393_-17-1139 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987366 | ||||||
chr2:147987368
|
G | A | 2 | a0002c0002t0002g0083a0002c0002t0002g0085 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17-11393C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987368 | ||||||
chr2:147987382
|
G | A | 126 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(123): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-17-11407C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987382 | ||||||
chr2:147987382
|
G | GTGTA | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(65): Show | 75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-17-11408_-17-1140 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987382 | ||||||
chr2:147987384
|
A | G | 17 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0196others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-11409T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987384 | ||||||
chr2:147987391
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(66): Show | 76 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-17-11416A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987391 | ||||||
chr2:147987391
|
T | TACAC | 8 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0211others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-11420_-17-1141 others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987391 | ||||||
chr2:147987393
|
C | T | 19 | a0001c0001t0003g0166a0001c0001t0005g0176a0001c0001t0006g0016others(16): Show | 20 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-11418G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987393 | ||||||
chr2:147987413
|
A | C | 168 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(165): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-17-11438T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987413 | ||||||
chr2:147987682
|
G | A | 1 | a0002c0002t0004g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-17-11707C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987682 | ||||||
chr2:147987830
|
G | T | 4 | a0002c0002t0002g0051a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-11855C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987830 | ||||||
chr2:147987850
|
G | A | 2 | a0001c0001t0047g0258a0001c0001t0059g0158 | 2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-17-11875C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987850 | ||||||
chr2:147987984
|
C | T | 3 | a0001c0001t0026g0018a0002c0002t0004g0029a0002c0002t0004g0030 | 3 | HG02895.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-17-12009G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147987984 | ||||||
chr2:147988006
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-17-12031A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988006 | ||||||
chr2:147988039
|
C | T | 1 | a0001c0001t0003g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-12064G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988039 | ||||||
chr2:147988213
|
C | T | 1 | a0001c0001t0012g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-17-12238G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988213 | ||||||
chr2:147988224
|
G | A | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-12249C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988224 | ||||||
chr2:147988291
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-17-12316T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988291 | ||||||
chr2:147988362
|
A | AT | 14 | a0001c0001t0001g0152a0001c0001t0005g0232a0001c0001t0006g0016others(11): Show | 15 | HG00642.hp2 HG02257.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-12388dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988362 | ||||||
chr2:147988390
|
C | T | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-12415G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988390 | ||||||
chr2:147988510
|
A | G | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-12535T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988510 | ||||||
chr2:147988516
|
C | T | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-12541G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988516 | ||||||
chr2:147988524
|
A | C | 1 | a0001c0001t0003g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-12549T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988524 | ||||||
chr2:147988618
|
G | A | 1 | a0002c0002t0009g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-17-12643C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988618 | ||||||
chr2:147988789
|
A | C | 1 | a0002c0002t0010g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-12814T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988789 | ||||||
chr2:147988792
|
C | CA | 113 | a0001c0001t0005g0167a0001c0001t0005g0307a0001c0001t0005g0308others(110): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-17-12818dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988792 | ||||||
chr2:147988792
|
C | CAA | 21 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(18): Show | 22 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-12819_-17-1281 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988792 | ||||||
chr2:147988792
|
CA | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(105): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-17-12818delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988792 | ||||||
chr2:147988987
|
T | C | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-13012A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147988987 | ||||||
chr2:147989124
|
A | G | 217 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(214): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-17-13149T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989124 | ||||||
chr2:147989223
|
G | T | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-13248C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989223 | ||||||
chr2:147989348
|
C | T | 1 | a0002c0002t0031g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-17-13373G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989348 | ||||||
chr2:147989406
|
A | T | 1 | a0001c0004t0007g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-17-13431T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989406 | ||||||
chr2:147989531
|
C | T | 1 | a0001c0001t0048g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-13556G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989531 | ||||||
chr2:147989639
|
G | A | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-13664C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989639 | ||||||
chr2:147989709
|
A | C | 3 | a0001c0001t0005g0307a0001c0001t0005g0308a0001c0001t0021g0306 | 3 | HG00735.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-13734T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989709 | ||||||
chr2:147989709
|
AAAC | A | 21 | a0001c0001t0006g0016a0001c0001t0008g0249a0001c0001t0008g0252others(18): Show | 22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17-13737_-17-1373 others(7): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989709 | ||||||
chr2:147989870
|
A | G | 168 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(165): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-17-13895T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147989870 | ||||||
chr2:147990284
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-14309A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990284 | ||||||
chr2:147990333
|
G | A | 8 | a0001c0001t0006g0014a0001c0001t0006g0243a0001c0001t0006g0246others(5): Show | 10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-14358C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990333 | ||||||
chr2:147990409
|
G | A | 39 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-14434C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990409 | ||||||
chr2:147990677
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-14702C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990677 | ||||||
chr2:147990696
|
T | C | 1 | a0002c0002t0002g0006 | 2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-17-14721A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990696 | ||||||
chr2:147990736
|
T | C | 1 | a0002c0002t0013g0060 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-17-14761A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990736 | ||||||
chr2:147990787
|
AGTTAAGT others(9): Show |
A | 1 | a0002c0002t0002g0111 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-17-14828_-17-1481 others(20): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990787 | ||||||
chr2:147990819
|
A | G | 1 | a0002c0002t0002g0086 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-17-14844T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147990819 | ||||||
chr2:147991008
|
A | G | 88 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(85): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-15033T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991008 | ||||||
chr2:147991050
|
C | CT | 80 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(77): Show | 83 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-17-15076dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991050 | ||||||
chr2:147991050
|
CT | C | 123 | a0001c0001t0001g0240a0002c0002t0002g0001a0002c0002t0002g0006others(120): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-17-15076delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991050 | ||||||
chr2:147991122
|
A | G | 2 | a0002c0002t0002g0088a0002c0002t0002g0098 | 2 | HG01943.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-17-15147T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991122 | ||||||
chr2:147991150
|
C | T | 1 | a0001c0001t0012g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-17-15175G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991150 | ||||||
chr2:147991208
|
C | T | 1 | a0002c0002t0033g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-17-15233G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991208 | ||||||
chr2:147991239
|
G | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-15264C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991239 | ||||||
chr2:147991398
|
G | A | 93 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(90): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-15423C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991398 | ||||||
chr2:147991458
|
T | C | 1 | a0002c0002t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-17-15483A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991458 | ||||||
chr2:147991490
|
G | A | 3 | a0002c0002t0002g0001a0002c0002t0002g0097a0002c0002t0002g0119 | 5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-15515C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991490 | ||||||
chr2:147991491
|
A | G | 3 | a0002c0002t0002g0001a0002c0002t0002g0097a0002c0002t0002g0119 | 5 | NA18952.hp2 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-15516T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991491 | ||||||
chr2:147991551
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-17-15576C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991551 | ||||||
chr2:147991698
|
C | T | 1 | a0001c0001t0001g0011 | 2 | NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-17-15723G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991698 | ||||||
chr2:147991766
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-17-15791A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991766 | ||||||
chr2:147991790
|
T | C | 5 | a0001c0001t0005g0167a0001c0001t0005g0307a0001c0001t0005g0308others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-15815A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991790 | ||||||
chr2:147991824
|
C | T | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-17-15849G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147991824 | ||||||
chr2:147992023
|
C | T | 30 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(27): Show | 33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-16048G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992023 | ||||||
chr2:147992254
|
C | T | 40 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(37): Show | 41 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-17-16279G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992254 | ||||||
chr2:147992401
|
T | A | 5 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(2): Show | 6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-16426A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992401 | ||||||
chr2:147992481
|
G | A | 1 | a0002c0002t0004g0037 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-16506C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992481 | ||||||
chr2:147992537
|
C | T | 1 | a0001c0001t0049g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-16562G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992537 | ||||||
chr2:147992557
|
GA | G | 5 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(2): Show | 6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-16583delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992557 | ||||||
chr2:147992575
|
A | G | 1 | a0002c0002t0004g0118 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-17-16600T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992575 | ||||||
chr2:147992675
|
G | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-16700C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992675 | ||||||
chr2:147992827
|
C | T | 2 | a0001c0001t0018g0265a0001c0001t0046g0262 | 2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17-16852G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992827 | ||||||
chr2:147992920
|
C | T | 1 | a0001c0001t0050g0244 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-17-16945G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992920 | ||||||
chr2:147992933
|
A | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-16958T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992933 | ||||||
chr2:147992940
|
T | C | 168 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(165): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-17-16965A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147992940 | ||||||
chr2:147993014
|
T | C | 1 | a0002c0002t0036g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-17-17039A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993014 | ||||||
chr2:147993018
|
C | T | 1 | a0001c0001t0051g0260 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17-17043G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993018 | ||||||
chr2:147993197
|
C | T | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-17222G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993197 | ||||||
chr2:147993544
|
C | T | 5 | a0001c0001t0005g0167a0001c0001t0005g0307a0001c0001t0005g0308others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-17569G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993544 | ||||||
chr2:147993996
|
T | G | 1 | a0002c0002t0002g0135 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-17-18021A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147993996 | ||||||
chr2:147994043
|
C | T | 88 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0007others(85): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-18068G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994043 | ||||||
chr2:147994233
|
A | T | 1 | a0001c0001t0003g0282 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-17-18258T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994233 | ||||||
chr2:147994322
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17-18347G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994322 | ||||||
chr2:147994862
|
T | A | 1 | a0001c0001t0042g0255 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-17-18887A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147994862 | ||||||
chr2:147995048
|
T | G | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-19073A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995048 | ||||||
chr2:147995118
|
CTGTAAAT others(121): Show |
C | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-19271_-17-1914 others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995118 | ||||||
chr2:147995193
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-17-19218G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995193 | ||||||
chr2:147995293
|
T | C | 206 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-17-19318A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995293 | ||||||
chr2:147995295
|
C | T | 1 | a0001c0001t0059g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-19320G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995295 | ||||||
chr2:147995363
|
TGTGGGGC others(46): Show |
T | 1 | a0002c0002t0027g0096 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-17-19441_-17-1938 others(57): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995363 | ||||||
chr2:147995417
|
G | A | 8 | a0001c0001t0003g0166a0001c0001t0014g0159a0001c0001t0014g0160others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-19442C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995417 | ||||||
chr2:147995451
|
C | T | 5 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(2): Show | 6 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-19476G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995451 | ||||||
chr2:147995581
|
C | G | 1 | a0001c0001t0047g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-19606G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995581 | ||||||
chr2:147995661
|
C | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-19686G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995661 | ||||||
chr2:147995751
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17-19776C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995751 | ||||||
chr2:147995787
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-19812G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995787 | ||||||
chr2:147995902
|
A | T | 1 | a0002c0002t0002g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-17-19927T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995902 | ||||||
chr2:147995932
|
A | G | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-19957T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995932 | ||||||
chr2:147995948
|
C | T | 1 | a0002c0002t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-17-19973G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995948 | ||||||
chr2:147995999
|
C | CA | 39 | a0001c0001t0001g0145a0001c0001t0001g0225a0001c0001t0003g0296others(36): Show | 40 | HG00099.hp2 HG00423.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-20025dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147995999 | ||||||
chr2:147996008
|
A | T | 1 | a0001c0001t0003g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-20033T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996008 | ||||||
chr2:147996059
|
C | T | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-20084G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996059 | ||||||
chr2:147996212
|
G | A | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0002g0129 | 3 | HG00323.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17-20237C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996212 | ||||||
chr2:147996239
|
A | C | 5 | a0001c0001t0003g0166a0001c0001t0014g0160a0001c0001t0014g0161others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-20264T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996239 | ||||||
chr2:147996245
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-17-20270T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996245 | ||||||
chr2:147996257
|
T | C | 2 | a0001c0001t0003g0292a0001c0001t0003g0293 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-17-20282A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996257 | ||||||
chr2:147996330
|
T | C | 1 | a0005c0006t0037g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-20355A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996330 | ||||||
chr2:147996400
|
C | T | 1 | a0001c0001t0023g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-17-20425G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996400 | ||||||
chr2:147996417
|
A | C | 10 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0253others(7): Show | 10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-20442T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996417 | ||||||
chr2:147996442
|
C | T | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-20467G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996442 | ||||||
chr2:147996637
|
G | A | 38 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(35): Show | 39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-17-20662C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996637 | ||||||
chr2:147996898
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-17-20923T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147996898 | ||||||
chr2:147997091
|
T | A | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-21116A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997091 | ||||||
chr2:147997164
|
A | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-21189T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997164 | ||||||
chr2:147997256
|
A | G | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-21281T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997256 | ||||||
chr2:147997293
|
T | G | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-21318A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997293 | ||||||
chr2:147997368
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17-21393T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997368 | ||||||
chr2:147997392
|
G | A | 1 | a0002c0002t0040g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-17-21417C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997392 | ||||||
chr2:147997450
|
T | A | 22 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(19): Show | 23 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-21475A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997450 | ||||||
chr2:147997541
|
A | C | 2 | a0002c0002t0002g0095a0002c0002t0002g0117 | 2 | HG00741.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-17-21566T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997541 | ||||||
chr2:147997668
|
C | T | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-21693G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997668 | ||||||
chr2:147997689
|
C | T | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-21714G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997689 | ||||||
chr2:147997820
|
G | A | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-21845C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997820 | ||||||
chr2:147997854
|
G | A | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-21879C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997854 | ||||||
chr2:147997857
|
A | G | 1 | a0002c0002t0004g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-17-21882T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997857 | ||||||
chr2:147997999
|
C | A | 1 | a0004c0005t0001g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-22024G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147997999 | ||||||
chr2:147998028
|
C | G | 21 | a0001c0001t0006g0016a0001c0001t0008g0249a0001c0001t0008g0252others(18): Show | 22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17-22053G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998028 | ||||||
chr2:147998099
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-17-22124A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998099 | ||||||
chr2:147998244
|
GA | G | 206 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-17-22270delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998244 | ||||||
chr2:147998272
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-22297G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998272 | ||||||
chr2:147998503
|
A | G | 35 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(32): Show | 36 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-18+22130T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998503 | ||||||
chr2:147998731
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+21902A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998731 | ||||||
chr2:147998753
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+21880A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998753 | ||||||
chr2:147998754
|
A | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+21879T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998754 | ||||||
chr2:147998929
|
C | T | 1 | a0001c0001t0055g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18+21704G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147998929 | ||||||
chr2:147999055
|
G | A | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-18+21578C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999055 | ||||||
chr2:147999099
|
A | T | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+21534T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999099 | ||||||
chr2:147999575
|
A | G | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+21058T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999575 | ||||||
chr2:147999874
|
G | C | 2 | a0002c0002t0002g0010a0002c0002t0002g0124 | 3 | HG02602.hp1 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-18+20759C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 147999874 | ||||||
chr2:148000077
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-18+20556T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000077 | ||||||
chr2:148000145
|
G | T | 1 | a0001c0001t0018g0265 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+20488C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000145 | ||||||
chr2:148000162
|
A | G | 4 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+20471T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000162 | ||||||
chr2:148000255
|
A | G | 36 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(33): Show | 37 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-18+20378T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000255 | ||||||
chr2:148000301
|
A | G | 125 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+20332T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000301 | ||||||
chr2:148000303
|
G | C | 4 | a0002c0002t0013g0060a0002c0002t0015g0076a0002c0002t0015g0077others(1): Show | 4 | HG00140.hp1 HG01884.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+20330C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000303 | ||||||
chr2:148000334
|
C | A | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+20299G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000334 | ||||||
chr2:148000583
|
C | T | 1 | a0001c0001t0021g0187 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-18+20050G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000583 | ||||||
chr2:148000623
|
T | C | 7 | a0001c0001t0003g0166a0001c0001t0014g0159a0001c0001t0014g0160others(4): Show | 7 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+20010A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000623 | ||||||
chr2:148000910
|
A | G | 89 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(86): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+19723T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148000910 | ||||||
chr2:148001066
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-18+19567C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001066 | ||||||
chr2:148001363
|
G | A | 1 | a0002c0002t0015g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18+19270C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001363 | ||||||
chr2:148001418
|
G | A | 1 | a0001c0001t0008g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+19215C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001418 | ||||||
chr2:148001581
|
G | A | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+19052C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001581 | ||||||
chr2:148001675
|
T | C | 2 | a0001c0001t0005g0173a0001c0001t0053g0226 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-18+18958A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001675 | ||||||
chr2:148001707
|
G | C | 4 | a0002c0002t0002g0010a0002c0002t0002g0114a0002c0002t0002g0115others(1): Show | 5 | HG01123.hp2 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+18926C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001707 | ||||||
chr2:148001779
|
T | C | 89 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(86): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+18854A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148001779 | ||||||
chr2:148002008
|
A | T | 1 | a0002c0002t0002g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+18625T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002008 | ||||||
chr2:148002087
|
A | G | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+18546T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002087 | ||||||
chr2:148002138
|
T | C | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+18495A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002138 | ||||||
chr2:148002144
|
C | T | 30 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(27): Show | 33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-18+18489G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002144 | ||||||
chr2:148002330
|
G | A | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+18303C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002330 | ||||||
chr2:148002347
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+18286C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002347 | ||||||
chr2:148002710
|
A | G | 1 | a0002c0002t0002g0093 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-18+17923T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002710 | ||||||
chr2:148002721
|
A | G | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+17912T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002721 | ||||||
chr2:148002929
|
A | G | 1 | a0001c0001t0012g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+17704T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148002929 | ||||||
chr2:148003049
|
A | G | 1 | a0002c0002t0033g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18+17584T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003049 | ||||||
chr2:148003057
|
C | T | 125 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+17576G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003057 | ||||||
chr2:148003058
|
C | T | 125 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+17575G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003058 | ||||||
chr2:148003084
|
A | T | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+17549T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003084 | ||||||
chr2:148003393
|
A | C | 1 | a0001c0001t0003g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-18+17240T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003393 | ||||||
chr2:148003400
|
A | G | 1 | a0005c0006t0037g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-18+17233T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003400 | ||||||
chr2:148003523
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+17110G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003523 | ||||||
chr2:148003539
|
C | T | 1 | a0002c0002t0004g0040 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-18+17094G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003539 | ||||||
chr2:148003642
|
A | G | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+16991T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003642 | ||||||
chr2:148003644
|
G | A | 1 | a0002c0002t0002g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-18+16989C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003644 | ||||||
chr2:148003756
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+16877C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003756 | ||||||
chr2:148003842
|
T | C | 2 | a0002c0002t0002g0079a0002c0002t0002g0080 | 2 | HG00280.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-18+16791A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003842 | ||||||
chr2:148003989
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-18+16644A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148003989 | ||||||
chr2:148004132
|
A | G | 2 | a0002c0002t0009g0091a0002c0002t0009g0092 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-18+16501T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004132 | ||||||
chr2:148004140
|
C | T | 2 | a0001c0001t0003g0292a0001c0001t0003g0293 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-18+16493G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004140 | ||||||
chr2:148004180
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0005g0147 | 2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+16453G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004180 | ||||||
chr2:148004182
|
G | A | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+16451C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004182 | ||||||
chr2:148004294
|
G | A | 4 | a0002c0002t0002g0051a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+16339C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004294 | ||||||
chr2:148004344
|
G | A | 1 | a0001c0001t0003g0273 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-18+16289C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004344 | ||||||
chr2:148004344
|
G | C | 3 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0232 | 3 | HG00642.hp2 HG00741.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-18+16289C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004344 | ||||||
chr2:148004494
|
T | C | 25 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18+16139A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004494 | ||||||
chr2:148004514
|
G | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+16119C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004514 | ||||||
chr2:148004548
|
G | T | 1 | a0001c0001t0041g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-18+16085C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004548 | ||||||
chr2:148004722
|
C | T | 1 | a0001c0001t0005g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+15911G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004722 | ||||||
chr2:148004879
|
T | C | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+15754A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004879 | ||||||
chr2:148004999
|
G | A | 125 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+15634C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148004999 | ||||||
chr2:148005201
|
A | C | 2 | a0003c0003t0020g0237a0003c0003t0020g0238 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+15432T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005201 | ||||||
chr2:148005224
|
C | T | 129 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(126): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-18+15409G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005224 | ||||||
chr2:148005354
|
A | T | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+15279T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005354 | ||||||
chr2:148005586
|
C | A | 2 | a0001c0001t0001g0218a0001c0001t0062g0188 | 2 | NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-18+15047G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005586 | ||||||
chr2:148005656
|
C | CA | 93 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 99 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-18+14976dupT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | ||||||
chr2:148005656
|
C | CAA | 43 | a0001c0001t0001g0003a0001c0001t0001g0146a0001c0001t0001g0149others(40): Show | 45 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-18+14975_-18+1497 others(6): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | ||||||
chr2:148005656
|
CA | C | 12 | a0001c0001t0041g0234a0001c0001t0043g0299a0002c0002t0004g0137others(9): Show | 12 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+14976delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | ||||||
chr2:148005656
|
CAAAAAAA others(4): Show |
C | 2 | a0002c0002t0002g0065a0002c0002t0002g0130 | 2 | HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-18+14966_-18+1497 others(15): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | ||||||
chr2:148005656
|
CAAAAAAA others(6): Show |
C | 1 | a0002c0002t0004g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18+14964_-18+1497 others(17): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005656 | ||||||
chr2:148005671
|
A | C | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+14962T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005671 | ||||||
chr2:148005676
|
A | C | 1 | a0001c0001t0008g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18+14957T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005676 | ||||||
chr2:148005750
|
G | A | 10 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(7): Show | 11 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+14883C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005750 | ||||||
chr2:148005788
|
C | A | 1 | a0001c0004t0007g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+14845G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005788 | ||||||
chr2:148005898
|
C | T | 1 | a0001c0001t0041g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-18+14735G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005898 | ||||||
chr2:148005900
|
C | A | 10 | a0001c0001t0003g0273a0001c0001t0003g0275a0001c0001t0003g0276others(7): Show | 10 | NA18943.hp1 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+14733G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148005900 | ||||||
chr2:148006040
|
C | A | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+14593G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006040 | ||||||
chr2:148006041
|
G | A | 4 | a0001c0001t0003g0017a0001c0001t0003g0274a0001c0001t0003g0298others(1): Show | 5 | HG01255.hp1 HG01358.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+14592C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006041 | ||||||
chr2:148006075
|
G | A | 1 | a0002c0002t0002g0065 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-18+14558C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006075 | ||||||
chr2:148006106
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+14527C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006106 | ||||||
chr2:148006203
|
C | T | 2 | a0002c0002t0002g0133a0002c0002t0031g0066 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-18+14430G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006203 | ||||||
chr2:148006290
|
T | A | 1 | a0001c0001t0008g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18+14343A>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006290 | ||||||
chr2:148006310
|
C | CA | 214 | a0001c0001t0003g0017a0001c0001t0003g0166a0001c0001t0003g0269others(211): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-18+14322_-18+1432 others(5): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006310 | ||||||
chr2:148006312
|
C | T | 8 | a0001c0001t0003g0166a0001c0001t0014g0159a0001c0001t0014g0160others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+14321G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006312 | ||||||
chr2:148006315
|
A | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(98): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18+14318T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006315 | ||||||
chr2:148006461
|
A | G | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+14172T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006461 | ||||||
chr2:148006476
|
G | A | 38 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(35): Show | 39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-18+14157C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006476 | ||||||
chr2:148006576
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+14057A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006576 | ||||||
chr2:148006634
|
G | A | 2 | a0003c0003t0020g0237a0003c0003t0020g0238 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-18+13999C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006634 | ||||||
chr2:148006644
|
C | T | 1 | a0002c0002t0031g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-18+13989G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006644 | ||||||
chr2:148006762
|
C | A | 25 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(22): Show | 26 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18+13871G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006762 | ||||||
chr2:148006784
|
G | C | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+13849C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006784 | ||||||
chr2:148006891
|
C | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+13742G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006891 | ||||||
chr2:148006892
|
C | G | 5 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(2): Show | 5 | HG00408.hp1 HG03486.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+13741G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006892 | ||||||
chr2:148006929
|
T | C | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+13704A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006929 | ||||||
chr2:148006986
|
T | G | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18+13647A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148006986 | ||||||
chr2:148007145
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-18+13488G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007145 | ||||||
chr2:148007321
|
C | T | 125 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+13312G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007321 | ||||||
chr2:148007525
|
A | G | 1 | a0002c0002t0002g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+13108T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007525 | ||||||
chr2:148007655
|
T | G | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+12978A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007655 | ||||||
chr2:148007857
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+12776T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007857 | ||||||
chr2:148007927
|
C | T | 90 | a0001c0001t0028g0112a0001c0001t0062g0188a0002c0002t0002g0001others(87): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-18+12706G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148007927 | ||||||
chr2:148008022
|
G | A | 2 | a0002c0002t0004g0029a0002c0002t0004g0030 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-18+12611C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008022 | ||||||
chr2:148008092
|
T | C | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+12541A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008092 | ||||||
chr2:148008150
|
A | C | 4 | a0001c0001t0001g0311a0001c0001t0005g0181a0001c0001t0005g0182others(1): Show | 4 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+12483T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008150 | ||||||
chr2:148008167
|
T | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0227others(1): Show | 4 | HG00558.hp1 NA18981.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+12466A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008167 | ||||||
chr2:148008247
|
A | T | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+12386T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008247 | ||||||
chr2:148008253
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+12380T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008253 | ||||||
chr2:148008315
|
A | T | 206 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-18+12318T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008315 | ||||||
chr2:148008439
|
T | G | 1 | a0002c0002t0002g0084 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18+12194A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008439 | ||||||
chr2:148008510
|
G | C | 22 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(19): Show | 23 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+12123C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008510 | ||||||
chr2:148008519
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+12114A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008519 | ||||||
chr2:148008530
|
G | A | 1 | a0001c0001t0003g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-18+12103C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008530 | ||||||
chr2:148008566
|
A | G | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+12067T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008566 | ||||||
chr2:148008842
|
C | T | 1 | a0002c0002t0040g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-18+11791G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008842 | ||||||
chr2:148008906
|
C | T | 125 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+11727G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148008906 | ||||||
chr2:148009018
|
G | A | 1 | a0003c0003t0011g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18+11615C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009018 | ||||||
chr2:148009054
|
G | A | 1 | a0002c0002t0004g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-18+11579C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009054 | ||||||
chr2:148009102
|
A | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+11531T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009102 | ||||||
chr2:148009249
|
A | G | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18+11384T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009249 | ||||||
chr2:148009347
|
T | C | 1 | a0001c0001t0021g0187 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-18+11286A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009347 | ||||||
chr2:148009522
|
A | G | 22 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(19): Show | 23 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+11111T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009522 | ||||||
chr2:148009657
|
G | C | 1 | a0003c0003t0011g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-18+10976C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009657 | ||||||
chr2:148009887
|
C | T | 2 | a0002c0002t0004g0061a0002c0002t0004g0125 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+10746G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148009887 | ||||||
chr2:148010103
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-18+10530G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010103 | ||||||
chr2:148010177
|
T | G | 1 | a0002c0002t0039g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+10456A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010177 | ||||||
chr2:148010252
|
G | T | 52 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(49): Show | 56 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18+10381C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010252 | ||||||
chr2:148010321
|
A | T | 1 | a0002c0002t0038g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18+10312T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010321 | ||||||
chr2:148010401
|
T | C | 1 | a0002c0002t0004g0045 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-18+10232A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010401 | ||||||
chr2:148010478
|
G | A | 9 | a0001c0001t0006g0016a0001c0001t0018g0264a0001c0001t0018g0265others(6): Show | 10 | HG02257.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+10155C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010478 | ||||||
chr2:148010545
|
T | C | 1 | a0002c0002t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+10088A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010545 | ||||||
chr2:148010598
|
C | T | 1 | a0001c0001t0012g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-18+10035G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010598 | ||||||
chr2:148010604
|
A | C | 1 | a0001c0001t0003g0281 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-18+10029T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010604 | ||||||
chr2:148010848
|
C | CT | 14 | a0001c0001t0003g0270a0001c0001t0006g0014a0001c0001t0006g0243others(11): Show | 15 | HG01884.hp2 HG01978.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+9784dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010848 | ||||||
chr2:148010848
|
CT | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(101): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+9784delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010848 | ||||||
chr2:148010848
|
CTTTTTT | C | 21 | a0002c0002t0004g0004a0002c0002t0004g0024a0002c0002t0004g0028others(18): Show | 22 | HG00423.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+9779_-18+9784d others(8): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010848 | ||||||
chr2:148010931
|
C | T | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+9702G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010931 | ||||||
chr2:148010932
|
G | C | 1 | a0001c0001t0003g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-18+9701C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010932 | ||||||
chr2:148010978
|
G | A | 3 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314 | 3 | NA18988.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-18+9655C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148010978 | ||||||
chr2:148011004
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9629A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011004 | ||||||
chr2:148011019
|
G | A | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+9614C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011019 | ||||||
chr2:148011117
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-18+9516G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011117 | ||||||
chr2:148011160
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-18+9473G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011160 | ||||||
chr2:148011304
|
T | C | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+9329A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011304 | ||||||
chr2:148011391
|
G | C | 1 | a0002c0002t0002g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+9242C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011391 | ||||||
chr2:148011415
|
A | G | 1 | a0002c0002t0034g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18+9218T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011415 | ||||||
chr2:148011446
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+9187C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011446 | ||||||
chr2:148011711
|
AACCTAAA others(4): Show |
A | 1 | a0001c0001t0035g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+8911_-18+8921d others(13): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011711 | ||||||
chr2:148011838
|
A | T | 3 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022 | 3 | HG00408.hp1 NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-18+8795T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011838 | ||||||
chr2:148011962
|
GAA | G | 2 | a0001c0001t0006g0016a0001c0001t0047g0258 | 3 | HG02723.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-18+8669_-18+8670d others(4): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011962 | ||||||
chr2:148011996
|
T | C | 8 | a0001c0001t0041g0234a0003c0003t0011g0143a0003c0003t0011g0233others(5): Show | 8 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+8637A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148011996 | ||||||
chr2:148012282
|
C | T | 1 | a0002c0002t0002g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-18+8351G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012282 | ||||||
chr2:148012485
|
C | A | 131 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(128): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-18+8148G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012485 | ||||||
chr2:148012537
|
T | C | 1 | a0002c0002t0002g0127 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-18+8096A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012537 | ||||||
chr2:148012618
|
A | G | 2 | a0001c0001t0005g0307a0001c0001t0021g0306 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+8015T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012618 | ||||||
chr2:148012663
|
T | C | 2 | a0001c0001t0003g0276a0001c0001t0043g0299 | 2 | NA18946.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-18+7970A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012663 | ||||||
chr2:148012705
|
G | T | 95 | a0001c0001t0028g0112a0001c0001t0035g0025a0002c0002t0002g0001others(92): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-18+7928C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012705 | ||||||
chr2:148012724
|
T | C | 1 | a0002c0002t0002g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+7909A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012724 | ||||||
chr2:148012740
|
C | T | 1 | a0001c0004t0007g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+7893G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012740 | ||||||
chr2:148012839
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7794A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012839 | ||||||
chr2:148012897
|
T | C | 7 | a0003c0003t0011g0143a0003c0003t0011g0233a0003c0003t0011g0235others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+7736A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148012897 | ||||||
chr2:148013071
|
A | T | 1 | a0001c0001t0045g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+7562T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013071 | ||||||
chr2:148013091
|
C | A | 1 | a0002c0002t0002g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-18+7542G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013091 | ||||||
chr2:148013248
|
TA | T | 11 | a0002c0002t0002g0027a0002c0002t0004g0004a0002c0002t0004g0024others(8): Show | 12 | HG00738.hp2 HG01175.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+7384delT | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013248 | ||||||
chr2:148013262
|
A | T | 1 | a0002c0002t0002g0086 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-18+7371T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013262 | ||||||
chr2:148013368
|
A | G | 30 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(27): Show | 33 | HG01167.hp1 HG01261.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-18+7265T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013368 | ||||||
chr2:148013400
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+7233T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013400 | ||||||
chr2:148013438
|
G | A | 1 | a0002c0002t0004g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-18+7195C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013438 | ||||||
chr2:148013483
|
T | C | 1 | a0001c0004t0006g0266 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+7150A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013483 | ||||||
chr2:148013860
|
C | T | 4 | a0001c0001t0003g0277a0001c0001t0003g0279a0001c0001t0003g0310others(1): Show | 4 | HG00733.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6773G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013860 | ||||||
chr2:148013967
|
T | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6666A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013967 | ||||||
chr2:148013998
|
G | A | 1 | a0001c0001t0003g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-18+6635C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148013998 | ||||||
chr2:148014122
|
T | G | 126 | a0001c0001t0028g0112a0001c0001t0035g0025a0002c0002t0002g0001others(123): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-18+6511A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014122 | ||||||
chr2:148014194
|
A | G | 21 | a0002c0002t0002g0007a0002c0002t0002g0071a0002c0002t0002g0072others(18): Show | 22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+6439T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014194 | ||||||
chr2:148014399
|
T | C | 1 | a0001c0004t0006g0266 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+6234A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014399 | ||||||
chr2:148014622
|
G | A | 1 | a0001c0001t0003g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18+6011C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014622 | ||||||
chr2:148014640
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18+5993T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014640 | ||||||
chr2:148014686
|
C | T | 2 | a0002c0002t0002g0135a0002c0002t0039g0139 | 2 | HG03471.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-18+5947G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014686 | ||||||
chr2:148014691
|
ATAAAAAA others(4793): Show |
A | 1 | a0002c0002t0002g0135 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-18+1142_-18+5941d others(2): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014691 | ||||||
chr2:148014918
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+5715C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014918 | ||||||
chr2:148014927
|
T | C | 1 | a0001c0004t0006g0266 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+5706A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014927 | ||||||
chr2:148014929
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-18+5704G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148014929 | ||||||
chr2:148015087
|
AC | A | 4 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+5545delG | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015087 | ||||||
chr2:148015091
|
C | T | 6 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0002g0068others(3): Show | 6 | NA18944.hp1 NA18986.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+5542G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015091 | ||||||
chr2:148015201
|
A | C | 2 | a0001c0001t0005g0176a0001c0001t0054g0175 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-18+5432T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015201 | ||||||
chr2:148015307
|
A | AT | 48 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0168others(45): Show | 50 | HG00673.hp2 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+5325dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015307 | ||||||
chr2:148015307
|
AT | A | 67 | a0001c0001t0001g0231a0001c0001t0003g0017a0001c0001t0003g0269others(64): Show | 69 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-18+5325delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015307 | ||||||
chr2:148015378
|
G | A | 10 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0253others(7): Show | 10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+5255C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015378 | ||||||
chr2:148015440
|
G | C | 1 | a0001c0001t0005g0232 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+5193C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015440 | ||||||
chr2:148015469
|
C | T | 4 | a0002c0002t0002g0051a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+5164G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015469 | ||||||
chr2:148015549
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA18981.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-18+5084G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015549 | ||||||
chr2:148015556
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-18+5077G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015556 | ||||||
chr2:148015674
|
C | CT | 9 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(6): Show | 9 | HG02129.hp2 HG02155.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+4958dupA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015674 | ||||||
chr2:148015674
|
CT | C | 37 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0243others(34): Show | 40 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18+4958delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015674 | ||||||
chr2:148015742
|
A | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG00544.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-18+4891T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015742 | ||||||
chr2:148015826
|
T | C | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+4807A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015826 | ||||||
chr2:148015849
|
A | T | 1 | a0001c0001t0035g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+4784T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015849 | ||||||
chr2:148015868
|
G | A | 4 | a0002c0002t0010g0048a0002c0002t0010g0049a0002c0002t0010g0050others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+4765C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015868 | ||||||
chr2:148015976
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+4657A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148015976 | ||||||
chr2:148016111
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0005g0147 | 2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+4522G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016111 | ||||||
chr2:148016134
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18+4499G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016134 | ||||||
chr2:148016173
|
C | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG01496.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-18+4460G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016173 | ||||||
chr2:148016258
|
G | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+4375C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016258 | ||||||
chr2:148016301
|
A | T | 2 | a0001c0001t0019g0301a0001c0001t0019g0302 | 2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-18+4332T>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016301 | ||||||
chr2:148016457
|
G | C | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+4176C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016457 | ||||||
chr2:148016622
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0005g0147 | 2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+4011G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016622 | ||||||
chr2:148016752
|
A | G | 4 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(1): Show | 4 | HG00408.hp1 NA18959.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3881T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016752 | ||||||
chr2:148016783
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-18+3850C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016783 | ||||||
chr2:148016868
|
A | G | 10 | a0001c0001t0008g0249a0001c0001t0008g0252a0001c0001t0008g0253others(7): Show | 10 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3765T>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148016868 | ||||||
chr2:148017410
|
G | C | 1 | a0001c0001t0022g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18+3223C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017410 | ||||||
chr2:148017475
|
C | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | NA18942.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-18+3158G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017475 | ||||||
chr2:148017539
|
G | A | 1 | a0002c0002t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+3094C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017539 | ||||||
chr2:148017634
|
T | C | 8 | a0001c0001t0006g0014a0001c0001t0006g0243a0001c0001t0006g0246others(5): Show | 10 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+2999A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017634 | ||||||
chr2:148017674
|
G | A | 1 | a0002c0002t0004g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-18+2959C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148017674 | ||||||
chr2:148018009
|
G | A | 6 | a0002c0002t0010g0005a0002c0002t0010g0048a0002c0002t0010g0049others(3): Show | 7 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+2624C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018009 | ||||||
chr2:148018198
|
C | A | 21 | a0001c0001t0006g0016a0001c0001t0008g0249a0001c0001t0008g0252others(18): Show | 22 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18+2435G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018198 | ||||||
chr2:148018311
|
T | C | 1 | a0001c0004t0007g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+2322A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018311 | ||||||
chr2:148018331
|
A | C | 1 | a0002c0002t0004g0024 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18+2302T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018331 | ||||||
chr2:148018368
|
G | A | 38 | a0001c0001t0003g0017a0001c0001t0003g0269a0001c0001t0003g0270others(35): Show | 39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-18+2265C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018368 | ||||||
chr2:148018579
|
TTATTATA others(1): Show |
T | 125 | a0001c0001t0028g0112a0001c0001t0035g0025a0002c0002t0002g0001others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+2046_-18+2053d others(10): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018579 | ||||||
chr2:148018619
|
G | A | 2 | a0001c0001t0019g0301a0001c0001t0019g0302 | 2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-18+2014C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018619 | ||||||
chr2:148018712
|
G | C | 3 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305 | 3 | HG01891.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+1921C>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018712 | ||||||
chr2:148018869
|
G | A | 125 | a0001c0001t0028g0112a0001c0001t0035g0025a0002c0002t0002g0001others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18+1764C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018869 | ||||||
chr2:148018988
|
AT | A | 3 | a0001c0001t0005g0307a0001c0001t0005g0308a0001c0001t0021g0306 | 3 | HG00735.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+1644delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148018988 | ||||||
chr2:148019029
|
G | A | 1 | a0001c0001t0003g0309 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+1604C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019029 | ||||||
chr2:148019052
|
AT | A | 93 | a0001c0001t0028g0112a0002c0002t0002g0001a0002c0002t0002g0006others(90): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-18+1580delA | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019052 | ||||||
chr2:148019207
|
G | A | 1 | a0001c0001t0003g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18+1426C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019207 | ||||||
chr2:148019224
|
G | T | 1 | a0002c0002t0002g0019 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-18+1409C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019224 | ||||||
chr2:148019290
|
A | C | 130 | a0001c0001t0012g0020a0001c0001t0012g0021a0001c0001t0012g0022others(127): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+1343T>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019290 | ||||||
chr2:148019388
|
G | A | 1 | a0002c0002t0004g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-18+1245C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019388 | ||||||
chr2:148019509
|
T | C | 1 | a0002c0002t0013g0136 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-18+1124A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019509 | ||||||
chr2:148019625
|
G | T | 1 | a0003c0003t0011g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-18+1008C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019625 | ||||||
chr2:148019746
|
T | C | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+887A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019746 | ||||||
chr2:148019808
|
T | G | 1 | a0001c0001t0001g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18+825A>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019808 | ||||||
chr2:148019816
|
T | TAAATCCT others(282): Show |
1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+816_-18+817ins others(289): Show |
ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019816 | ||||||
chr2:148019999
|
G | A | 3 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314 | 3 | NA18988.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-18+634C>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148019999 | ||||||
chr2:148020100
|
C | G | 1 | a0001c0001t0026g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+533G>C | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020100 | ||||||
chr2:148020278
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18+355C>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020278 | ||||||
chr2:148020471
|
T | C | 1 | a0002c0002t0004g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-18+162A>G | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020471 | ||||||
chr2:148020474
|
C | A | 2 | a0001c0001t0001g0315a0001c0001t0001g0316 | 2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-18+159G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020474 | ||||||
chr2:148020497
|
C | A | 1 | a0002c0002t0029g0138 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-18+136G>T | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020497 | ||||||
chr2:148020569
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-18+64G>A | ORC4 | ENSG00000115947.14 | transcript | ENST00000392857.10 | protein_coding | 1/13 | chr2 | 148020569 |