geneid | 113510 |
---|---|
ensemblid | ENSG00000163312.11 |
hgncid | 18536 |
symbol | HELQ |
name | helicase, POLQ like |
refseq_nuc | NM_133636.5 |
refseq_prot | NP_598375.3 |
ensembl_nuc | ENST00000295488.8 |
ensembl_prot | ENSP00000295488.3 |
mane_status | MANE Select |
chr | chr4 |
start | 83407346 |
end | 83455823 |
strand | - |
ver | v1.2 |
region | chr4:83407346-83455823 |
region5000 | chr4:83402346-83460823 |
regionname0 | HELQ_chr4_83407346_83455823 |
regionname5000 | HELQ_chr4_83402346_83460823 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1101 | 148 | 21 | 29 | 74 | 4 | 19 | 51 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0002 | 0/0 | 1101 | 99 | 14 | 20 | 46 | 5 | 14 | 39 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003 | 0/0 | 1101 | 29 | 28 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004 | 0/0 | 1101 | 20 | 18 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0005 | 0/0 | 1101 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0006 | 0/0 | 1101 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0007 | 0/0 | 1101 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0008 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0009 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0010 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0011 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0012 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0013 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0014 | 1/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0015 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3306 | 125 | 10 | 24 | 73 | 2 | 15 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0002 | 0/0 | 3306 | 98 | 14 | 20 | 46 | 5 | 13 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0003 | 0/0 | 3306 | 27 | 26 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0004 | 0/0 | 3306 | 17 | 7 | 5 | 0 | 2 | 3 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0005 | 0/0 | 3306 | 15 | 13 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0006 | 0/0 | 3306 | 4 | 2 | 0 | 1 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0007 | 0/0 | 3306 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0008 | 0/0 | 3306 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0009 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0010 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0011 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0012 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0013 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0014 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0015 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0016 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0017 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0018 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0019 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0020 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0021 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0022 | 1/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0023 | 0/0 | 3306 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
c0024 | 0/0 | 3306 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 1 | 1 | 7 | 0 | 3 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3306 | 125 | 10 | 24 | 73 | 2 | 15 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0004 | 0/0 | 3306 | 17 | 7 | 5 | 0 | 2 | 3 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0006 | 0/0 | 3306 | 4 | 2 | 0 | 1 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0019 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0020 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0002c0002 | 0/0 | 3306 | 98 | 14 | 20 | 46 | 5 | 13 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0002c0021 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003c0003 | 0/0 | 3306 | 27 | 26 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003c0015 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003c0016 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0005 | 0/0 | 3306 | 15 | 13 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0010 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0011 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0005c0007 | 0/0 | 3306 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0006c0008 | 0/0 | 3306 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0007c0009 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0008c0012 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0009c0023 | 0/0 | 3306 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0010c0018 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0011c0017 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0012c0014 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0013c0013 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0014c0022 | 1/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0015c0024 | 0/0 | 3306 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3543 | 125 | 10 | 24 | 73 | 2 | 15 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0004t0001 | 0/0 | 3543 | 17 | 7 | 5 | 0 | 2 | 3 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0006t0001 | 0/0 | 3543 | 4 | 2 | 0 | 1 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0019t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0001c0020t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0002c0002t0001 | 0/0 | 3543 | 98 | 14 | 20 | 46 | 5 | 13 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0002c0021t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003c0003t0002 | 0/0 | 3540 | 27 | 26 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003c0015t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0003c0016t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0005t0001 | 0/0 | 3543 | 11 | 10 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0005t0002 | 0/0 | 3540 | 4 | 3 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0010t0001 | 0/0 | 3543 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0004c0011t0002 | 0/0 | 3540 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0005c0007t0001 | 0/0 | 3543 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0006c0008t0001 | 0/0 | 3543 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0007c0009t0002 | 0/0 | 3540 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0008c0012t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0009c0023t0001 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0010c0018t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0011c0017t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0012c0014t0002 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0013c0013t0002 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0014c0022t0001 | 1/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
a0015c0024t0001 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | copy fasta | chr4 | 83402346 | 83460823 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0006t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0006t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0019t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0020t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0001 | 0/0 | 12 | 1 | 1 | 7 | 0 | 3 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0021t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0015t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0016t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0010t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0010t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0011t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0011t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0005c0007t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0005c0007t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0005c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0007c0009t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0007c0009t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0008c0012t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0008c0012t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0009c0023t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0010c0018t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0011c0017t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0012c0014t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0013c0013t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0014c0022t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0015c0024t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0077 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0047 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0020 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0094 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0020 | EUR | FIN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00280 | hp2 | a0010 | c0018 | t0001 | g0143 | EUR | FIN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0109 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00733 | hp1 | a0001 | c0004 | t0001 | g0106 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0111 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0110 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01106 | hp1 | a0015 | c0024 | t0001 | g0229 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01109 | hp1 | a0003 | c0003 | t0002 | g0254 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01167 | hp2 | a0004 | c0005 | t0002 | g0257 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01243 | hp2 | a0004 | c0005 | t0001 | g0100 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0108 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0066 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0069 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01981 | hp2 | a0009 | c0023 | t0001 | g0228 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02055 | hp1 | a0004 | c0005 | t0001 | g0096 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02055 | hp2 | a0013 | c0013 | t0002 | g0255 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02080 | hp1 | a0001 | c0006 | t0001 | g0176 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02145 | hp2 | a0003 | c0003 | t0002 | g0233 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02258 | hp1 | a0001 | c0020 | t0001 | g0123 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02258 | hp2 | a0003 | c0003 | t0002 | g0247 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02451 | hp1 | a0003 | c0016 | t0001 | g0105 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02451 | hp2 | a0004 | c0010 | t0001 | g0224 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02572 | hp2 | a0003 | c0003 | t0002 | g0235 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02615 | hp1 | a0004 | c0005 | t0001 | g0019 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0030 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02622 | hp1 | a0008 | c0012 | t0001 | g0053 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02622 | hp2 | a0003 | c0003 | t0002 | g0011 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02630 | hp1 | a0003 | c0003 | t0002 | g0245 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02630 | hp2 | a0004 | c0005 | t0001 | g0019 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02717 | hp1 | a0004 | c0010 | t0001 | g0225 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02717 | hp2 | a0004 | c0011 | t0002 | g0232 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02723 | hp1 | a0003 | c0003 | t0002 | g0250 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02723 | hp2 | a0001 | c0019 | t0001 | g0157 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02738 | hp2 | a0011 | c0017 | t0001 | g0145 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02809 | hp2 | a0004 | c0005 | t0002 | g0032 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02818 | hp2 | a0004 | c0005 | t0001 | g0095 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02895 | hp1 | a0003 | c0003 | t0002 | g0258 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02895 | hp2 | a0004 | c0005 | t0001 | g0098 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02896 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02896 | hp2 | a0004 | c0005 | t0001 | g0099 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02897 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0244 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02922 | hp1 | a0003 | c0003 | t0002 | g0249 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02965 | hp1 | a0003 | c0003 | t0002 | g0234 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0120 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0121 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02970 | hp2 | a0003 | c0003 | t0002 | g0030 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02976 | hp2 | a0003 | c0003 | t0002 | g0011 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03041 | hp2 | a0005 | c0007 | t0001 | g0028 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03098 | hp1 | a0005 | c0007 | t0001 | g0223 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03098 | hp2 | a0007 | c0009 | t0002 | g0256 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03130 | hp1 | a0003 | c0003 | t0002 | g0011 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03130 | hp2 | a0003 | c0003 | t0002 | g0237 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03139 | hp1 | a0003 | c0003 | t0002 | g0252 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03139 | hp2 | a0004 | c0005 | t0002 | g0230 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03195 | hp1 | a0005 | c0007 | t0001 | g0114 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03195 | hp2 | a0003 | c0003 | t0002 | g0248 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03209 | hp1 | a0007 | c0009 | t0002 | g0031 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0104 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03225 | hp2 | a0003 | c0003 | t0002 | g0236 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03239 | hp2 | a0001 | c0006 | t0001 | g0178 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03453 | hp1 | a0004 | c0005 | t0002 | g0032 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03453 | hp2 | a0005 | c0007 | t0001 | g0028 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03486 | hp1 | a0003 | c0003 | t0002 | g0238 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03486 | hp2 | a0004 | c0005 | t0001 | g0102 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03516 | hp1 | a0006 | c0008 | t0001 | g0124 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03540 | hp1 | a0006 | c0008 | t0001 | g0122 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03540 | hp2 | a0004 | c0005 | t0001 | g0097 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03579 | hp2 | a0004 | c0005 | t0001 | g0101 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03654 | hp2 | a0002 | c0021 | t0001 | g0033 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03669 | hp2 | a0001 | c0004 | t0001 | g0112 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0107 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0113 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0013 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18906 | hp1 | a0003 | c0003 | t0002 | g0242 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18906 | hp2 | a0006 | c0008 | t0001 | g0117 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19030 | hp2 | a0003 | c0003 | t0002 | g0240 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19043 | hp1 | a0007 | c0009 | t0002 | g0031 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19240 | hp1 | a0003 | c0003 | t0002 | g0243 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19240 | hp2 | a0004 | c0011 | t0002 | g0231 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20129 | hp1 | a0003 | c0003 | t0002 | g0251 | AFR | ASW | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02486 | hp1 | a0012 | c0014 | t0002 | g0253 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0115 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0241 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03471 | hp1 | a0003 | c0003 | t0002 | g0239 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03471 | hp2 | a0006 | c0008 | t0001 | g0119 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0118 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG06807 | hp2 | a0004 | c0010 | t0001 | g0226 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20300 | hp1 | a0008 | c0012 | t0001 | g0054 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA21309 | hp1 | a0003 | c0003 | t0002 | g0246 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA21309 | hp2 | a0003 | c0015 | t0001 | g0103 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0222 | REF | REF | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
homoSapiens_grch38 | hp1 | a0014 | c0022 | t0001 | g0227 | REF | REF | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83407479
|
C | T | 2 | a0006a0012 | 5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.3280G>A | p.Val1094Met | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 18/18 | 3410/3543 | 3280/3306 | 1094/1101 | chr4 | 83407479 | ||
chr4:83427592
|
T | C | 1 | a0010 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2647A>G | p.Asn883Asp | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/18 | 2777/3543 | 2647/3306 | 883/1101 | chr4 | 83427592 | ||
chr4:83427612
|
T | A | 1 | a0005 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2627A>T | p.Tyr876Phe | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/18 | 2757/3543 | 2627/3306 | 876/1101 | chr4 | 83427612 | ||
chr4:83429586
|
T | C | 1 | a0007 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.2456A>G | p.Lys819Arg | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/18 | 2586/3543 | 2456/3306 | 819/1101 | chr4 | 83429586 | ||
chr4:83437005
|
C | T | 1 | a0005 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.1901G>A | p.Arg634His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/18 | 2031/3543 | 1901/3306 | 634/1101 | chr4 | 83437005 | ||
chr4:83437074
|
T | C | 1 | a0007 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1832A>G | p.Lys611Arg | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/18 | 1962/3543 | 1832/3306 | 611/1101 | chr4 | 83437074 | ||
chr4:83439918
|
G | A | 2 | a0003a0012 | 30 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(27): Show |
missense_variant | MODERATE | c.1753C>T | p.Pro585Ser | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/18 | 1883/3543 | 1753/3306 | 585/1101 | chr4 | 83439918 | ||
chr4:83441313
|
T | G | 1 | a0008 | 2 | HG02622.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.1654A>C | p.Asn552His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/18 | 1784/3543 | 1654/3306 | 552/1101 | chr4 | 83441313 | ||
chr4:83441321
|
C | T | 1 | a0008 | 2 | HG02622.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.1646G>A | p.Arg549His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/18 | 1776/3543 | 1646/3306 | 549/1101 | chr4 | 83441321 | ||
chr4:83443597
|
C | T | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1483G>A | p.Gly495Ser | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/18 | 1613/3543 | 1483/3306 | 495/1101 | chr4 | 83443597 | ||
chr4:83453327
|
C | T | 12 | a0001a0003a0004others(9): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
missense_variant | MODERATE | c.916G>A | p.Val306Ile | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 1046/3543 | 916/3306 | 306/1101 | chr4 | 83453327 | ||
chr4:83453539
|
A | G | 5 | a0003a0004a0007others(2): Show | 54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
missense_variant | MODERATE | c.704T>C | p.Leu235Pro | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 834/3543 | 704/3306 | 235/1101 | chr4 | 83453539 | ||
chr4:83453873
|
C | G | 1 | a0013 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.370G>C | p.Asp124His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 500/3543 | 370/3306 | 124/1101 | chr4 | 83453873 | ||
chr4:83455590
|
A | T | 14 | a0001a0002a0003others(11): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
missense_variant | MODERATE | c.104T>A | p.Val35Glu | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 234/3543 | 104/3306 | 35/1101 | chr4 | 83455590 | ||
chr4:83455594
|
G | A | 1 | a0009 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.100C>T | p.Leu34Phe | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 230/3543 | 100/3306 | 34/1101 | chr4 | 83455594 | ||
chr4:83455641
|
T | C | 1 | a0015 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.53A>G | p.Asn18Ser | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 183/3543 | 53/3306 | 18/1101 | chr4 | 83455641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83429717
|
A | G | 7 | a0001c0020a0003c0003a0003c0015others(4): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
synonymous_variant | LOW | c.2325T>C | p.His775His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/18 | 2455/3543 | 2325/3306 | 775/1101 | chr4 | 83429717 | ||
chr4:83443598
|
A | G | 11 | a0001c0001a0001c0019a0002c0021others(8): Show | 164 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(161): Show |
synonymous_variant | LOW | c.1482T>C | p.Ile494Ile | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/18 | 1612/3543 | 1482/3306 | 494/1101 | chr4 | 83443598 | ||
chr4:83448938
|
A | G | 6 | a0001c0001a0001c0006a0009c0023others(3): Show | 133 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(130): Show |
synonymous_variant | LOW | c.1036T>C | p.Leu346Leu | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/18 | 1166/3543 | 1036/3306 | 346/1101 | chr4 | 83448938 | ||
chr4:83453538
|
C | A | 1 | a0003c0016 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.705G>T | p.Leu235Leu | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 835/3543 | 705/3306 | 235/1101 | chr4 | 83453538 | ||
chr4:83455586
|
G | C | 1 | a0004c0010 | 3 | HG02451.hp2 HG02717.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.108C>G | p.Pro36Pro | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 238/3543 | 108/3306 | 36/1101 | chr4 | 83455586 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83455719
|
ACGT | A | 6 | a0003c0003t0002a0004c0005t0002a0004c0011t0002others(3): Show | 38 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-29_-27delACG | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 27 | chr4 | 83455719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83407581
|
G | A | 6 | a0002c0002t0001g0066a0002c0002t0001g0077a0002c0002t0001g0078others(3): Show | 6 | HG00099.hp1 HG00733.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.3199-21C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407581 | ||||||
chr4:83407700
|
G | A | 1 | a0002c0002t0001g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3199-140C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407700 | ||||||
chr4:83407748
|
T | G | 1 | a0003c0016t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3199-188A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407748 | ||||||
chr4:83407906
|
A | G | 1 | a0001c0019t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3199-346T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407906 | ||||||
chr4:83407929
|
G | A | 16 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(13): Show | 19 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.3199-369C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407929 | ||||||
chr4:83407951
|
T | G | 5 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0122others(2): Show | 5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-391A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407951 | ||||||
chr4:83408046
|
A | G | 31 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(28): Show | 34 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.3199-486T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408046 | ||||||
chr4:83408134
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3199-574A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408134 | ||||||
chr4:83408197
|
T | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0155a0001c0001t0001g0206others(19): Show | 26 | HG01081.hp2 HG01106.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3199-637A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408197 | ||||||
chr4:83408291
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3199-731G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408291 | ||||||
chr4:83408494
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3199-934C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408494 | ||||||
chr4:83408652
|
G | A | 1 | a0001c0004t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3199-1092C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408652 | ||||||
chr4:83408701
|
C | T | 5 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0122others(2): Show | 5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-1141G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408701 | ||||||
chr4:83408762
|
G | C | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3199-1202C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408762 | ||||||
chr4:83408906
|
A | G | 16 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(13): Show | 19 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.3199-1346T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408906 | ||||||
chr4:83408961
|
G | A | 3 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0124 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-1401C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408961 | ||||||
chr4:83409047
|
A | C | 5 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0122others(2): Show | 5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-1487T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409047 | ||||||
chr4:83409054
|
T | C | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0140others(4): Show | 7 | NA18952.hp1 NA18954.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.3199-1494A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409054 | ||||||
chr4:83409201
|
T | C | 6 | a0001c0006t0001g0022a0002c0002t0001g0029a0002c0002t0001g0055others(3): Show | 8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3199-1641A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409201 | ||||||
chr4:83409322
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0155a0001c0001t0001g0206others(11): Show | 16 | HG01081.hp2 HG01106.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3199-1762C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409322 | ||||||
chr4:83409424
|
G | A | 1 | a0004c0005t0001g0099 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3199-1864C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409424 | ||||||
chr4:83409550
|
T | C | 5 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0122others(2): Show | 5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-1990A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409550 | ||||||
chr4:83409553
|
CA | C | 23 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(20): Show | 26 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.3199-1994delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409553 | ||||||
chr4:83409578
|
C | A | 53 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(50): Show | 59 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.3199-2018G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409578 | ||||||
chr4:83409830
|
C | T | 1 | a0008c0012t0001g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3199-2270G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409830 | ||||||
chr4:83410034
|
T | C | 1 | a0004c0005t0001g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3199-2474A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410034 | ||||||
chr4:83410051
|
G | A | 6 | a0001c0006t0001g0022a0002c0002t0001g0029a0002c0002t0001g0055others(3): Show | 8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3199-2491C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410051 | ||||||
chr4:83410153
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3199-2593T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410153 | ||||||
chr4:83410221
|
C | T | 2 | a0001c0004t0001g0116a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3199-2661G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410221 | ||||||
chr4:83410230
|
C | CA | 6 | a0001c0006t0001g0022a0002c0002t0001g0029a0002c0002t0001g0055others(3): Show | 8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3199-2671dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410230 | ||||||
chr4:83410289
|
A | C | 55 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(52): Show | 62 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.3199-2729T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410289 | ||||||
chr4:83410290
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3199-2730A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410290 | ||||||
chr4:83410392
|
T | C | 3 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0124 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-2832A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410392 | ||||||
chr4:83410458
|
G | T | 3 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0124 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-2898C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410458 | ||||||
chr4:83410518
|
C | CAG | 53 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(50): Show | 59 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.3199-2960_3199-295 others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410518 | ||||||
chr4:83410542
|
G | A | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3199-2982C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410542 | ||||||
chr4:83410572
|
G | A | 1 | a0003c0003t0002g0246 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3199-3012C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410572 | ||||||
chr4:83410615
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.3199-3055A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410615 | ||||||
chr4:83410645
|
G | A | 5 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0122others(2): Show | 5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-3085C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410645 | ||||||
chr4:83410712
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3199-3152C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410712 | ||||||
chr4:83410836
|
T | C | 90 | a0001c0001t0001g0155a0001c0001t0001g0206a0001c0001t0001g0207others(87): Show | 101 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.3199-3276A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410836 | ||||||
chr4:83410960
|
G | A | 1 | a0003c0003t0002g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3199-3400C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410960 | ||||||
chr4:83410985
|
T | TA | 6 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0218others(3): Show | 6 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.3199-3426dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410985 | ||||||
chr4:83411087
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3199-3527C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411087 | ||||||
chr4:83411157
|
C | CA | 40 | a0001c0001t0001g0130a0001c0001t0001g0153a0001c0001t0001g0155others(37): Show | 44 | HG01081.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.3199-3598dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411157 | ||||||
chr4:83411157
|
CA | C | 53 | a0001c0001t0001g0148a0001c0004t0001g0020a0001c0004t0001g0106others(50): Show | 60 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.3199-3598delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411157 | ||||||
chr4:83411206
|
T | C | 3 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0124 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-3646A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411206 | ||||||
chr4:83411251
|
T | C | 52 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(49): Show | 59 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.3199-3691A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411251 | ||||||
chr4:83411310
|
A | T | 2 | a0002c0002t0001g0069a0002c0002t0001g0070 | 2 | HG01070.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3199-3750T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411310 | ||||||
chr4:83411321
|
T | C | 1 | a0002c0002t0001g0039 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3199-3761A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411321 | ||||||
chr4:83411604
|
A | AAAAT | 31 | a0001c0006t0001g0022a0001c0019t0001g0157a0002c0002t0001g0029others(28): Show | 36 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.3199-4048_3199-404 others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411604 | ||||||
chr4:83411625
|
A | AAATAAAT others(4): Show |
1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3199-4066_3199-406 others(15): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411625 | ||||||
chr4:83411630
|
T | A | 1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3199-4070A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411630 | ||||||
chr4:83411637
|
T | A | 3 | a0002c0002t0001g0081a0002c0002t0001g0089a0002c0002t0001g0090 | 3 | HG03017.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3199-4077A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411637 | ||||||
chr4:83411953
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3199-4393C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411953 | ||||||
chr4:83412178
|
T | G | 5 | a0004c0005t0001g0097a0004c0005t0001g0098a0004c0010t0001g0224others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3198+4553A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412178 | ||||||
chr4:83412185
|
T | C | 1 | a0004c0005t0002g0230 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3198+4546A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412185 | ||||||
chr4:83412311
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3198+4420G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412311 | ||||||
chr4:83412314
|
G | A | 3 | a0006c0008t0001g0117a0006c0008t0001g0119a0006c0008t0001g0124 | 3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3198+4417C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412314 | ||||||
chr4:83412395
|
G | A | 13 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(10): Show | 14 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3198+4336C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412395 | ||||||
chr4:83412726
|
A | T | 1 | a0002c0002t0001g0069 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3198+4005T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412726 | ||||||
chr4:83412817
|
C | G | 12 | a0001c0004t0001g0115a0001c0006t0001g0022a0002c0002t0001g0029others(9): Show | 14 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3198+3914G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412817 | ||||||
chr4:83412912
|
G | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 9 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3198+3819C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412912 | ||||||
chr4:83413135
|
C | G | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3198+3596G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413135 | ||||||
chr4:83413153
|
T | C | 27 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(24): Show | 30 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.3198+3578A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413153 | ||||||
chr4:83413365
|
C | T | 1 | a0012c0014t0002g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3198+3366G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413365 | ||||||
chr4:83413566
|
T | C | 1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3198+3165A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413566 | ||||||
chr4:83413593
|
C | T | 1 | a0001c0004t0001g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3198+3138G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413593 | ||||||
chr4:83413614
|
C | G | 51 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(48): Show | 57 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3198+3117G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413614 | ||||||
chr4:83413818
|
A | G | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 38 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(35): Show |
intron_variant | MODIFIER | c.3198+2913T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413818 | ||||||
chr4:83413860
|
G | T | 10 | a0001c0006t0001g0022a0002c0002t0001g0029a0002c0002t0001g0051others(7): Show | 12 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3198+2871C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413860 | ||||||
chr4:83414003
|
T | C | 1 | a0002c0002t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3198+2728A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414003 | ||||||
chr4:83414064
|
C | T | 1 | a0002c0002t0001g0065 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3198+2667G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414064 | ||||||
chr4:83414324
|
A | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0155a0001c0001t0001g0206others(3): Show | 7 | HG01081.hp2 HG01106.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3198+2407T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414324 | ||||||
chr4:83414421
|
A | G | 4 | a0005c0007t0001g0028a0005c0007t0001g0223a0007c0009t0002g0031others(1): Show | 6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3198+2310T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414421 | ||||||
chr4:83414441
|
C | T | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3198+2290G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414441 | ||||||
chr4:83414487
|
GC | G | 3 | a0001c0020t0001g0123a0008c0012t0001g0053a0008c0012t0001g0054 | 3 | HG02258.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3198+2243delG | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414487 | ||||||
chr4:83414827
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3198+1904C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414827 | ||||||
chr4:83414844
|
C | G | 1 | a0004c0011t0002g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3198+1887G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414844 | ||||||
chr4:83415128
|
C | T | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 38 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(35): Show |
intron_variant | MODIFIER | c.3198+1603G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415128 | ||||||
chr4:83415130
|
C | T | 84 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(81): Show | 95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.3198+1601G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415130 | ||||||
chr4:83415329
|
T | C | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3198+1402A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415329 | ||||||
chr4:83415388
|
A | G | 4 | a0005c0007t0001g0028a0005c0007t0001g0223a0007c0009t0002g0031others(1): Show | 6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3198+1343T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415388 | ||||||
chr4:83415495
|
C | T | 4 | a0005c0007t0001g0028a0005c0007t0001g0223a0007c0009t0002g0031others(1): Show | 6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3198+1236G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415495 | ||||||
chr4:83415636
|
C | CT | 31 | a0001c0001t0001g0154a0001c0001t0001g0182a0001c0004t0001g0116others(28): Show | 34 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.3198+1094dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415636 | ||||||
chr4:83415676
|
A | G | 14 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.3198+1055T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415676 | ||||||
chr4:83415686
|
G | A | 5 | a0004c0005t0001g0096a0004c0005t0001g0100a0004c0005t0001g0101others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3198+1045C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415686 | ||||||
chr4:83415767
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3198+964C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415767 | ||||||
chr4:83415810
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3198+921G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415810 | ||||||
chr4:83415922
|
T | C | 84 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(81): Show | 95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.3198+809A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415922 | ||||||
chr4:83415941
|
C | T | 1 | a0002c0002t0001g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3198+790G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415941 | ||||||
chr4:83415946
|
CA | C | 13 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(10): Show | 15 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.3198+784delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415946 | ||||||
chr4:83415947
|
A | AT | 12 | a0001c0001t0001g0146a0001c0001t0001g0165a0001c0001t0001g0179others(9): Show | 13 | HG01109.hp1 HG02080.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3198+783dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | ||||||
chr4:83415947
|
A | T | 1 | a0013c0013t0002g0255 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3198+784T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | ||||||
chr4:83415947
|
AT | A | 30 | a0001c0004t0001g0021a0001c0004t0001g0115a0001c0004t0001g0116others(27): Show | 32 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.3198+783delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | ||||||
chr4:83415947
|
ATT | A | 7 | a0001c0006t0001g0022a0002c0002t0001g0029a0002c0002t0001g0055others(4): Show | 9 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3198+782_3198+783d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | ||||||
chr4:83416015
|
C | T | 13 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(10): Show | 14 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3198+716G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416015 | ||||||
chr4:83416072
|
G | A | 29 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3198+659C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416072 | ||||||
chr4:83416092
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0160others(2): Show | 7 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3198+639C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416092 | ||||||
chr4:83416250
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3198+481A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416250 | ||||||
chr4:83416255
|
T | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0211a0015c0024t0001g0229 | 3 | HG01081.hp2 HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3198+476A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416255 | ||||||
chr4:83416463
|
C | T | 1 | a0002c0002t0001g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3198+268G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416463 | ||||||
chr4:83416579
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3198+152G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416579 | ||||||
chr4:83416594
|
C | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3198+137G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416594 | ||||||
chr4:83416923
|
T | C | 14 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.3064-58A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83416923 | ||||||
chr4:83416994
|
C | T | 2 | a0001c0001t0001g0144a0010c0018t0001g0143 | 2 | HG00280.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3064-129G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83416994 | ||||||
chr4:83417078
|
C | G | 29 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3064-213G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417078 | ||||||
chr4:83417149
|
T | C | 4 | a0005c0007t0001g0028a0005c0007t0001g0223a0007c0009t0002g0031others(1): Show | 6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3064-284A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417149 | ||||||
chr4:83417348
|
G | T | 1 | a0002c0002t0001g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3064-483C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417348 | ||||||
chr4:83417560
|
C | G | 29 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3063+533G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417560 | ||||||
chr4:83417572
|
G | A | 1 | a0001c0004t0001g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3063+521C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417572 | ||||||
chr4:83417818
|
C | T | 27 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(24): Show | 30 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.3063+275G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417818 | ||||||
chr4:83417833
|
C | T | 29 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3063+260G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417833 | ||||||
chr4:83418059
|
A | C | 1 | a0001c0006t0001g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3063+34T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83418059 | ||||||
chr4:83418357
|
G | C | 1 | a0001c0001t0001g0026 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2950-151C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418357 | ||||||
chr4:83418454
|
T | C | 2 | a0005c0007t0001g0028a0005c0007t0001g0223 | 3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2950-248A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418454 | ||||||
chr4:83418673
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2950-467T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418673 | ||||||
chr4:83418809
|
C | T | 1 | a0001c0004t0001g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2950-603G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418809 | ||||||
chr4:83418923
|
T | C | 1 | a0002c0002t0001g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2950-717A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418923 | ||||||
chr4:83418972
|
G | A | 2 | a0005c0007t0001g0028a0005c0007t0001g0223 | 3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2950-766C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418972 | ||||||
chr4:83419083
|
CCACAGGC others(2): Show |
C | 4 | a0001c0004t0001g0116a0004c0005t0002g0230a0006c0008t0001g0122others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-886_2950-878d others(11): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419083 | ||||||
chr4:83419093
|
C | T | 4 | a0001c0004t0001g0116a0004c0005t0002g0230a0006c0008t0001g0122others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-887G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419093 | ||||||
chr4:83419094
|
A | G | 4 | a0001c0004t0001g0116a0004c0005t0002g0230a0006c0008t0001g0122others(1): Show | 4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-888T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419094 | ||||||
chr4:83419161
|
A | AT | 32 | a0001c0001t0001g0194a0001c0020t0001g0123a0003c0003t0002g0011others(29): Show | 36 | HG01109.hp1 HG01175.hp2 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.2950-956dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419161 | ||||||
chr4:83419161
|
AT | A | 39 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(36): Show | 44 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2950-956delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419161 | ||||||
chr4:83419161
|
ATT | A | 11 | a0001c0004t0001g0021a0001c0004t0001g0116a0001c0004t0001g0118others(8): Show | 12 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.2950-957_2950-956d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419161 | ||||||
chr4:83419192
|
G | A | 1 | a0003c0003t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2950-986C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419192 | ||||||
chr4:83419198
|
G | C | 6 | a0001c0006t0001g0022a0002c0002t0001g0029a0002c0002t0001g0055others(3): Show | 8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-992C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419198 | ||||||
chr4:83419392
|
A | G | 1 | a0006c0008t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2950-1186T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419392 | ||||||
chr4:83419395
|
C | T | 1 | a0004c0005t0001g0099 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2950-1189G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419395 | ||||||
chr4:83419478
|
T | C | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-1272A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419478 | ||||||
chr4:83419726
|
C | T | 7 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(4): Show | 8 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-1520G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419726 | ||||||
chr4:83419743
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2950-1537A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419743 | ||||||
chr4:83419768
|
C | T | 12 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(9): Show | 14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2950-1562G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419768 | ||||||
chr4:83419804
|
C | G | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-1598G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419804 | ||||||
chr4:83419988
|
A | C | 29 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.2949+1575T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419988 | ||||||
chr4:83420028
|
G | A | 26 | a0001c0020t0001g0123a0003c0003t0002g0030a0003c0003t0002g0233others(23): Show | 28 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.2949+1535C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420028 | ||||||
chr4:83420075
|
A | G | 2 | a0005c0007t0001g0114a0005c0007t0001g0223 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2949+1488T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420075 | ||||||
chr4:83420343
|
G | A | 6 | a0002c0002t0001g0029a0002c0002t0001g0055a0002c0002t0001g0071others(3): Show | 7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2949+1220C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420343 | ||||||
chr4:83420413
|
G | A | 3 | a0001c0001t0001g0147a0001c0004t0001g0107a0001c0004t0001g0108 | 3 | HG01255.hp1 HG03688.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2949+1150C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420413 | ||||||
chr4:83420434
|
C | T | 5 | a0001c0004t0001g0021a0001c0004t0001g0118a0001c0004t0001g0121others(2): Show | 6 | HG02922.hp2 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2949+1129G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420434 | ||||||
chr4:83420468
|
C | T | 1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2949+1095G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420468 | ||||||
chr4:83420684
|
T | C | 44 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(41): Show | 50 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.2949+879A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420684 | ||||||
chr4:83420704
|
G | A | 29 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(26): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2949+859C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420704 | ||||||
chr4:83420710
|
G | A | 27 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(24): Show | 30 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2949+853C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420710 | ||||||
chr4:83420712
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2949+851C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420712 | ||||||
chr4:83420717
|
G | A | 2 | a0005c0007t0001g0028a0005c0007t0001g0223 | 3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2949+846C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420717 | ||||||
chr4:83420983
|
T | C | 1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2949+580A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420983 | ||||||
chr4:83420996
|
T | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2949+567A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420996 | ||||||
chr4:83421116
|
T | C | 1 | a0002c0002t0001g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2949+447A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421116 | ||||||
chr4:83421132
|
G | A | 1 | a0002c0002t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2949+431C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421132 | ||||||
chr4:83421161
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2949+402T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421161 | ||||||
chr4:83421189
|
C | CAA | 3 | a0001c0001t0001g0192a0002c0002t0001g0007a0002c0002t0001g0038 | 5 | NA18959.hp2 NA18968.hp2 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.2949+372_2949+373d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421189 | ||||||
chr4:83421232
|
T | G | 1 | a0002c0002t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2949+331A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421232 | ||||||
chr4:83421359
|
G | T | 7 | a0001c0004t0001g0021a0001c0004t0001g0118a0001c0004t0001g0120others(4): Show | 8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2949+204C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421359 | ||||||
chr4:83421461
|
C | A | 1 | a0002c0002t0001g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2949+102G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421461 | ||||||
chr4:83421543
|
C | T | 1 | a0001c0006t0001g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2949+20G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421543 | ||||||
chr4:83422351
|
C | T | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2776-615G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422351 | ||||||
chr4:83422411
|
C | T | 84 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(81): Show | 95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.2776-675G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422411 | ||||||
chr4:83422460
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0142others(10): Show | 17 | HG00609.hp1 HG02165.hp1 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.2776-724T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422460 | ||||||
chr4:83422504
|
A | G | 10 | a0001c0004t0001g0021a0001c0004t0001g0116a0001c0004t0001g0118others(7): Show | 11 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.2776-768T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422504 | ||||||
chr4:83422776
|
G | A | 28 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(25): Show | 31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2776-1040C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422776 | ||||||
chr4:83422857
|
A | G | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2776-1121T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422857 | ||||||
chr4:83422942
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2776-1206C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422942 | ||||||
chr4:83423082
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2776-1346G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423082 | ||||||
chr4:83423094
|
T | C | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2776-1358A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423094 | ||||||
chr4:83423164
|
A | G | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2776-1428T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423164 | ||||||
chr4:83423210
|
A | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0139a0001c0001t0001g0209others(1): Show | 6 | HG00558.hp2 HG01952.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2776-1474T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423210 | ||||||
chr4:83423245
|
C | T | 1 | a0006c0008t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2776-1509G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423245 | ||||||
chr4:83423263
|
T | C | 2 | a0005c0007t0001g0028a0005c0007t0001g0223 | 3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2776-1527A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423263 | ||||||
chr4:83423273
|
A | T | 1 | a0002c0002t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2776-1537T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423273 | ||||||
chr4:83423500
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2776-1764A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423500 | ||||||
chr4:83423614
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(26): Show | 32 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.2776-1878C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423614 | ||||||
chr4:83423651
|
T | C | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2776-1915A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423651 | ||||||
chr4:83423685
|
C | T | 1 | a0001c0004t0001g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2776-1949G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423685 | ||||||
chr4:83423723
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2776-1987G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423723 | ||||||
chr4:83423727
|
A | G | 12 | a0001c0004t0001g0115a0001c0006t0001g0022a0002c0002t0001g0029others(9): Show | 14 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2776-1991T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423727 | ||||||
chr4:83423763
|
T | G | 8 | a0001c0004t0001g0021a0001c0004t0001g0115a0001c0004t0001g0118others(5): Show | 9 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2776-2027A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423763 | ||||||
chr4:83423780
|
G | A | 1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2776-2044C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423780 | ||||||
chr4:83423800
|
A | T | 3 | a0001c0020t0001g0123a0008c0012t0001g0053a0008c0012t0001g0054 | 3 | HG02258.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2776-2064T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423800 | ||||||
chr4:83423902
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+2092C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423902 | ||||||
chr4:83423996
|
A | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0212 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2775+1998T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423996 | ||||||
chr4:83424020
|
T | C | 2 | a0004c0005t0002g0230a0006c0008t0001g0122 | 2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2775+1974A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424020 | ||||||
chr4:83424054
|
C | A | 1 | a0002c0002t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2775+1940G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424054 | ||||||
chr4:83424112
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2775+1882A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424112 | ||||||
chr4:83424167
|
A | G | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+1827T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424167 | ||||||
chr4:83424273
|
T | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+1721A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424273 | ||||||
chr4:83424362
|
C | G | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2775+1632G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424362 | ||||||
chr4:83424381
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2775+1613G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424381 | ||||||
chr4:83424403
|
C | T | 1 | a0002c0002t0001g0012 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2775+1591G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424403 | ||||||
chr4:83424463
|
G | A | 3 | a0002c0002t0001g0077a0002c0002t0001g0079a0002c0002t0001g0080 | 3 | HG00099.hp1 HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2775+1531C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424463 | ||||||
chr4:83424543
|
G | A | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2775+1451C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424543 | ||||||
chr4:83424582
|
A | G | 2 | a0001c0001t0001g0206a0015c0024t0001g0229 | 2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2775+1412T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424582 | ||||||
chr4:83424958
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2775+1036A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424958 | ||||||
chr4:83424982
|
A | G | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2775+1012T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424982 | ||||||
chr4:83425050
|
C | G | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2775+944G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425050 | ||||||
chr4:83425152
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2775+842G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425152 | ||||||
chr4:83425258
|
C | T | 2 | a0006c0008t0001g0117a0006c0008t0001g0124 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2775+736G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425258 | ||||||
chr4:83425279
|
C | CA | 8 | a0001c0001t0001g0171a0001c0001t0001g0193a0001c0001t0001g0194others(5): Show | 8 | HG01175.hp2 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+714dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425279 | ||||||
chr4:83425279
|
C | CAA | 26 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(23): Show | 29 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.2775+713_2775+714d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425279 | ||||||
chr4:83425279
|
CA | C | 52 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0106others(49): Show | 60 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2775+714delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425279 | ||||||
chr4:83425365
|
GA | G | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2775+628delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425365 | ||||||
chr4:83425539
|
T | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+455A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425539 | ||||||
chr4:83425575
|
T | G | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2775+419A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425575 | ||||||
chr4:83425859
|
G | A | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2775+135C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425859 | ||||||
chr4:83425958
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0160others(2): Show | 7 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2775+36T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425958 | ||||||
chr4:83426126
|
C | A | 1 | a0001c0004t0001g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2677-34G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426126 | ||||||
chr4:83426210
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 131 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.2677-118T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426210 | ||||||
chr4:83426247
|
TAGGATAT others(4): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2677-166_2677-156d others(13): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426247 | ||||||
chr4:83426270
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 171 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.2677-178G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426270 | ||||||
chr4:83426572
|
G | GT | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(82): Show | 103 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.2677-481dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426572 | ||||||
chr4:83426583
|
TG | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(25): Show | 31 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2677-492delC | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426583 | ||||||
chr4:83426585
|
A | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(25): Show | 31 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2677-493T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426585 | ||||||
chr4:83426650
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2677-558C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426650 | ||||||
chr4:83426772
|
C | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 171 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.2677-680G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426772 | ||||||
chr4:83426796
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 132 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.2677-704G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426796 | ||||||
chr4:83426824
|
C | T | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2677-732G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426824 | ||||||
chr4:83426920
|
T | G | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676+643A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426920 | ||||||
chr4:83426941
|
T | C | 1 | a0002c0002t0001g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2676+622A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426941 | ||||||
chr4:83427043
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676+520C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427043 | ||||||
chr4:83427074
|
A | G | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2676+489T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427074 | ||||||
chr4:83427154
|
T | C | 1 | a0001c0001t0001g0025 | 2 | NA18959.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2676+409A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427154 | ||||||
chr4:83427188
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2676+375T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427188 | ||||||
chr4:83427249
|
A | G | 4 | a0002c0002t0001g0063a0002c0002t0001g0081a0002c0002t0001g0089others(1): Show | 4 | HG02004.hp1 HG03017.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676+314T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427249 | ||||||
chr4:83427376
|
C | T | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2676+187G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427376 | ||||||
chr4:83427957
|
G | A | 2 | a0004c0005t0002g0230a0006c0008t0001g0122 | 2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2519-237C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83427957 | ||||||
chr4:83428074
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 132 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.2519-354A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428074 | ||||||
chr4:83428089
|
T | G | 1 | a0012c0014t0002g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2519-369A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428089 | ||||||
chr4:83428334
|
C | A | 1 | a0012c0014t0002g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2519-614G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428334 | ||||||
chr4:83428358
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2519-638T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428358 | ||||||
chr4:83428378
|
T | C | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2519-658A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428378 | ||||||
chr4:83428434
|
C | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 170 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.2519-714G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428434 | ||||||
chr4:83428601
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2519-881T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428601 | ||||||
chr4:83428712
|
C | G | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2518+812G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428712 | ||||||
chr4:83428782
|
T | C | 2 | a0002c0002t0001g0079a0002c0002t0001g0080 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2518+742A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428782 | ||||||
chr4:83428799
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2518+725A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428799 | ||||||
chr4:83428833
|
AAATG | A | 10 | a0001c0004t0001g0021a0001c0004t0001g0116a0001c0004t0001g0118others(7): Show | 11 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.2518+687_2518+690d others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428833 | ||||||
chr4:83428903
|
G | T | 3 | a0003c0003t0002g0244a0003c0003t0002g0245a0003c0003t0002g0258 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2518+621C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428903 | ||||||
chr4:83428953
|
A | G | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2518+571T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428953 | ||||||
chr4:83429019
|
T | C | 2 | a0002c0002t0001g0071a0002c0002t0001g0072 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2518+505A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429019 | ||||||
chr4:83429056
|
CT | C | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2518+467delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429056 | ||||||
chr4:83429176
|
C | T | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2518+348G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429176 | ||||||
chr4:83429217
|
A | G | 1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2518+307T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429217 | ||||||
chr4:83429292
|
A | G | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2518+232T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429292 | ||||||
chr4:83429434
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2518+90G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429434 | ||||||
chr4:83429501
|
A | G | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2518+23T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429501 | ||||||
chr4:83429763
|
T | C | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2296-17A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83429763 | ||||||
chr4:83429832
|
C | T | 1 | a0002c0002t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2296-86G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83429832 | ||||||
chr4:83429900
|
T | C | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2296-154A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83429900 | ||||||
chr4:83430000
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.2296-254C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430000 | ||||||
chr4:83430131
|
C | T | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-385G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430131 | ||||||
chr4:83430146
|
A | C | 2 | a0003c0003t0002g0244a0003c0003t0002g0258 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2296-400T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430146 | ||||||
chr4:83430156
|
TA | T | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-411delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430156 | ||||||
chr4:83430175
|
A | G | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2296-429T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430175 | ||||||
chr4:83430274
|
T | TA | 29 | a0001c0001t0001g0184a0001c0020t0001g0123a0003c0003t0002g0011others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.2296-529dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430274 | ||||||
chr4:83430274
|
T | TAA | 5 | a0003c0015t0001g0103a0003c0016t0001g0105a0005c0007t0001g0028others(2): Show | 6 | HG02451.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-530_2296-529d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430274 | ||||||
chr4:83430315
|
GA | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 169 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.2296-570delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430315 | ||||||
chr4:83430348
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2296-602C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430348 | ||||||
chr4:83430406
|
G | T | 1 | a0012c0014t0002g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2296-660C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430406 | ||||||
chr4:83430451
|
C | T | 1 | a0013c0013t0002g0255 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2296-705G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430451 | ||||||
chr4:83430569
|
C | T | 1 | a0001c0004t0001g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2296-823G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430569 | ||||||
chr4:83430754
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2295+910A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430754 | ||||||
chr4:83431020
|
T | A | 1 | a0003c0016t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2295+644A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431020 | ||||||
chr4:83431108
|
A | AAAAC | 29 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(26): Show | 32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.2295+552_2295+555d others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431108 | ||||||
chr4:83431197
|
G | GT | 32 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(29): Show | 36 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2295+466dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431197 | ||||||
chr4:83431267
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2295+397T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431267 | ||||||
chr4:83431548
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2295+116A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431548 | ||||||
chr4:83431580
|
T | C | 1 | a0002c0002t0001g0048 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2295+84A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431580 | ||||||
chr4:83431597
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 131 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.2295+67A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431597 | ||||||
chr4:83432001
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 130 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.2190+125A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 10/17 | chr4 | 83432001 | ||||||
chr4:83432020
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2190+106A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 10/17 | chr4 | 83432020 | ||||||
chr4:83432073
|
A | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0186a0001c0001t0001g0190others(3): Show | 7 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.2190+53T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 10/17 | chr4 | 83432073 | ||||||
chr4:83432367
|
C | T | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2049-100G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432367 | ||||||
chr4:83432453
|
ACT | A | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2049-188_2049-187d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432453 | ||||||
chr4:83432642
|
C | T | 1 | a0001c0019t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2049-375G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432642 | ||||||
chr4:83432886
|
A | AAACAAC | 3 | a0001c0001t0001g0129a0001c0001t0001g0163a0001c0001t0001g0204 | 3 | NA18947.hp1 NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2049-625_2049-620d others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432886 | ||||||
chr4:83432971
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2049-704C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432971 | ||||||
chr4:83433061
|
T | TA | 26 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(23): Show | 29 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.2049-795dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433061 | ||||||
chr4:83433102
|
A | T | 1 | a0006c0008t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2049-835T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433102 | ||||||
chr4:83433139
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2049-872C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433139 | ||||||
chr4:83433212
|
T | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 132 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.2049-945A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433212 | ||||||
chr4:83433392
|
G | A | 28 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(25): Show | 31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2049-1125C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433392 | ||||||
chr4:83433441
|
G | A | 12 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(9): Show | 14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2049-1174C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433441 | ||||||
chr4:83433542
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2049-1275A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433542 | ||||||
chr4:83433558
|
C | T | 1 | a0001c0006t0001g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2049-1291G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433558 | ||||||
chr4:83433665
|
C | CA | 26 | a0001c0001t0001g0127a0001c0001t0001g0151a0001c0001t0001g0199others(23): Show | 29 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.2049-1399dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433665 | ||||||
chr4:83433665
|
CA | C | 36 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(33): Show | 39 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.2049-1399delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433665 | ||||||
chr4:83433710
|
T | C | 1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2049-1443A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433710 | ||||||
chr4:83433840
|
A | G | 1 | a0004c0005t0001g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2049-1573T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433840 | ||||||
chr4:83433843
|
T | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2049-1576A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433843 | ||||||
chr4:83433888
|
G | A | 28 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(25): Show | 31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2049-1621C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433888 | ||||||
chr4:83433895
|
C | T | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2049-1628G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433895 | ||||||
chr4:83433979
|
C | CA | 45 | a0001c0001t0001g0150a0001c0020t0001g0123a0002c0002t0001g0061others(42): Show | 50 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.2049-1713dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433979 | ||||||
chr4:83433985
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2049-1718T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433985 | ||||||
chr4:83433997
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2049-1730C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433997 | ||||||
chr4:83434091
|
C | T | 1 | a0002c0002t0001g0039 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2049-1824G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434091 | ||||||
chr4:83434129
|
G | A | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2049-1862C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434129 | ||||||
chr4:83434192
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2049-1925C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434192 | ||||||
chr4:83434471
|
A | AT | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 36 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2049-2205dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434471 | ||||||
chr4:83434619
|
T | G | 12 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(9): Show | 14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2048+2239A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434619 | ||||||
chr4:83434788
|
T | C | 1 | a0002c0002t0001g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2048+2070A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434788 | ||||||
chr4:83434848
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2048+2010C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434848 | ||||||
chr4:83434858
|
T | C | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2048+2000A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434858 | ||||||
chr4:83434922
|
A | G | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2048+1936T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434922 | ||||||
chr4:83434997
|
T | C | 35 | a0001c0006t0001g0178a0002c0002t0001g0001a0002c0002t0001g0004others(32): Show | 52 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.2048+1861A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434997 | ||||||
chr4:83435207
|
A | G | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2048+1651T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435207 | ||||||
chr4:83435256
|
A | G | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2048+1602T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435256 | ||||||
chr4:83435301
|
A | G | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2048+1557T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435301 | ||||||
chr4:83435538
|
C | T | 1 | a0004c0005t0001g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2048+1320G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435538 | ||||||
chr4:83435575
|
TA | T | 34 | a0001c0001t0001g0208a0001c0020t0001g0123a0003c0003t0002g0011others(31): Show | 38 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(35): Show |
intron_variant | MODIFIER | c.2048+1282delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435575 | ||||||
chr4:83435585
|
A | G | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2048+1273T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435585 | ||||||
chr4:83435637
|
A | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2048+1221T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435637 | ||||||
chr4:83435925
|
G | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 169 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.2048+933C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435925 | ||||||
chr4:83435935
|
A | C | 1 | a0002c0002t0001g0038 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2048+923T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435935 | ||||||
chr4:83435955
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2048+903T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435955 | ||||||
chr4:83435973
|
C | CA | 28 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(25): Show | 31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2048+884dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435973 | ||||||
chr4:83435973
|
CA | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2048+884delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435973 | ||||||
chr4:83435987
|
G | A | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2048+871C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435987 | ||||||
chr4:83436202
|
T | C | 1 | a0012c0014t0002g0253 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2048+656A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436202 | ||||||
chr4:83436241
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 169 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.2048+617G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436241 | ||||||
chr4:83436307
|
A | C | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2048+551T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436307 | ||||||
chr4:83436380
|
T | C | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2048+478A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436380 | ||||||
chr4:83436390
|
G | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2048+468C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436390 | ||||||
chr4:83436662
|
G | A | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2048+196C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436662 | ||||||
chr4:83436823
|
G | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2048+35C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436823 | ||||||
chr4:83437261
|
C | A | 2 | a0002c0002t0001g0073a0002c0002t0001g0074 | 2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1809-164G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437261 | ||||||
chr4:83437333
|
C | A | 3 | a0002c0002t0001g0017a0002c0002t0001g0068a0002c0002t0001g0087 | 4 | HG02132.hp1 NA18969.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-236G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437333 | ||||||
chr4:83437361
|
T | C | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1809-264A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437361 | ||||||
chr4:83437369
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1809-272A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437369 | ||||||
chr4:83437603
|
T | TA | 28 | a0001c0001t0001g0187a0001c0001t0001g0195a0001c0001t0001g0217others(25): Show | 31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1809-507dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437603 | ||||||
chr4:83437603
|
TA | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(59): Show | 69 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1809-507delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437603 | ||||||
chr4:83437604
|
A | T | 1 | a0002c0002t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1809-507T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437604 | ||||||
chr4:83437650
|
A | T | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-553T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437650 | ||||||
chr4:83437744
|
T | C | 1 | a0003c0003t0002g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1809-647A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437744 | ||||||
chr4:83437815
|
T | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-718A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437815 | ||||||
chr4:83437852
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1809-755A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437852 | ||||||
chr4:83437866
|
C | T | 33 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(30): Show | 37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1809-769G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437866 | ||||||
chr4:83437991
|
G | C | 2 | a0002c0002t0001g0043a0002c0002t0001g0044 | 2 | NA18953.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1809-894C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437991 | ||||||
chr4:83438272
|
T | C | 30 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(27): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.1809-1175A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438272 | ||||||
chr4:83438577
|
T | A | 28 | a0001c0020t0001g0123a0003c0003t0002g0011a0003c0003t0002g0030others(25): Show | 31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1808+1286A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438577 | ||||||
chr4:83438634
|
T | C | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+1229A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438634 | ||||||
chr4:83438641
|
C | G | 1 | a0002c0002t0001g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1808+1222G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438641 | ||||||
chr4:83438747
|
G | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+1116C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438747 | ||||||
chr4:83438748
|
G | GAAAAAA | 15 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(12): Show | 18 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1808+1109_1808+111 others(10): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | ||||||
chr4:83438748
|
G | GAAAAAAA | 32 | a0001c0004t0001g0116a0003c0003t0002g0011a0003c0003t0002g0030others(29): Show | 36 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.1808+1108_1808+111 others(11): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | ||||||
chr4:83438748
|
G | GAAAAAAA others(1): Show |
17 | a0001c0004t0001g0021a0001c0004t0001g0115a0001c0004t0001g0118others(14): Show | 18 | HG01109.hp1 HG02258.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1808+1107_1808+111 others(12): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | ||||||
chr4:83438748
|
GAA | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 129 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.1808+1113_1808+111 others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | ||||||
chr4:83438931
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 170 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.1808+932C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438931 | ||||||
chr4:83439192
|
C | A | 25 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(22): Show | 28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1808+671G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439192 | ||||||
chr4:83439267
|
ATGTTGGC others(287): Show |
A | 2 | a0003c0003t0002g0237a0003c0003t0002g0242 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1808+302_1808+595d others(2): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439267 | ||||||
chr4:83439313
|
C | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+550G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439313 | ||||||
chr4:83439367
|
C | CT | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 131 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1808+495dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439367 | ||||||
chr4:83439401
|
G | A | 5 | a0003c0015t0001g0103a0003c0016t0001g0105a0005c0007t0001g0028others(2): Show | 6 | HG02451.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1808+462C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439401 | ||||||
chr4:83439420
|
T | G | 1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1808+443A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439420 | ||||||
chr4:83439448
|
C | T | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1808+415G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439448 | ||||||
chr4:83439452
|
C | A | 12 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(9): Show | 14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1808+411G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439452 | ||||||
chr4:83439545
|
G | A | 1 | a0003c0003t0002g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1808+318C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439545 | ||||||
chr4:83439561
|
G | A | 4 | a0003c0003t0002g0238a0005c0007t0001g0028a0005c0007t0001g0114others(1): Show | 5 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1808+302C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439561 | ||||||
chr4:83439687
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1808+176G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439687 | ||||||
chr4:83439838
|
G | A | 1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1808+25C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439838 | ||||||
chr4:83440297
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1663-289A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440297 | ||||||
chr4:83440312
|
T | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-304A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440312 | ||||||
chr4:83440387
|
C | T | 2 | a0005c0007t0001g0028a0005c0007t0001g0223 | 3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1663-379G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440387 | ||||||
chr4:83440388
|
G | A | 2 | a0003c0003t0002g0244a0003c0003t0002g0258 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1663-380C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440388 | ||||||
chr4:83440792
|
G | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 166 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1662+513C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440792 | ||||||
chr4:83440800
|
G | T | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+505C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440800 | ||||||
chr4:83440902
|
C | T | 25 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(22): Show | 28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1662+403G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440902 | ||||||
chr4:83441106
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+199C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441106 | ||||||
chr4:83441248
|
T | G | 8 | a0001c0004t0001g0021a0001c0004t0001g0115a0001c0004t0001g0118others(5): Show | 9 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1662+57A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441248 | ||||||
chr4:83441281
|
G | A | 2 | a0002c0002t0001g0069a0002c0002t0001g0070 | 2 | HG01070.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1662+24C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441281 | ||||||
chr4:83441290
|
T | C | 50 | a0001c0004t0001g0020a0001c0004t0001g0021a0001c0004t0001g0107others(47): Show | 57 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1662+15A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441290 | ||||||
chr4:83441290
|
T | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 167 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.1662+15A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441290 | ||||||
chr4:83441298
|
A | G | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1662+7T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441298 | ||||||
chr4:83441299
|
T | C | 30 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(27): Show | 34 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.1662+6A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441299 | ||||||
chr4:83441435
|
G | A | 3 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0004t0001g0112 | 3 | HG00642.hp1 HG00741.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1564-32C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441435 | ||||||
chr4:83441770
|
C | T | 2 | a0007c0009t0002g0031a0007c0009t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1564-367G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441770 | ||||||
chr4:83441770
|
CT | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(53): Show | 70 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1564-368delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441770 | ||||||
chr4:83441922
|
C | T | 1 | a0001c0019t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1564-519G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441922 | ||||||
chr4:83442047
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1564-644C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442047 | ||||||
chr4:83442259
|
A | G | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564-856T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442259 | ||||||
chr4:83442260
|
A | AT | 49 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(46): Show | 54 | HG00609.hp2 HG00735.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1564-858dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | ||||||
chr4:83442260
|
A | ATT | 90 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(87): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1564-859_1564-858d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | ||||||
chr4:83442260
|
A | ATTT | 31 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0164others(28): Show | 34 | HG01109.hp1 HG01433.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1564-860_1564-858d others(5): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | ||||||
chr4:83442260
|
AT | A | 6 | a0002c0002t0001g0014a0002c0002t0001g0017a0002c0002t0001g0049others(3): Show | 8 | HG00140.hp2 HG01168.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-858delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | ||||||
chr4:83442423
|
ATGCTCTA others(222): Show |
A | 1 | a0003c0003t0002g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1563+865_1564-1021 others(3): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442423 | ||||||
chr4:83442426
|
C | G | 11 | a0001c0004t0001g0021a0001c0004t0001g0116a0001c0004t0001g0118others(8): Show | 12 | HG02258.hp1 HG02922.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1564-1023G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442426 | ||||||
chr4:83442448
|
C | G | 29 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(26): Show | 33 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1564-1045G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442448 | ||||||
chr4:83442485
|
G | T | 1 | a0011c0017t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1563+1032C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442485 | ||||||
chr4:83442496
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1563+1021G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442496 | ||||||
chr4:83442659
|
C | T | 27 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(24): Show | 30 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1563+858G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442659 | ||||||
chr4:83442702
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 133 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1563+815G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442702 | ||||||
chr4:83442800
|
C | T | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1563+717G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442800 | ||||||
chr4:83442844
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1563+673T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442844 | ||||||
chr4:83442956
|
G | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 137 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1563+561C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442956 | ||||||
chr4:83442995
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1563+522T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442995 | ||||||
chr4:83443091
|
T | C | 1 | a0004c0010t0001g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1563+426A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443091 | ||||||
chr4:83443340
|
C | A | 3 | a0003c0003t0002g0244a0003c0003t0002g0245a0003c0003t0002g0258 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1563+177G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443340 | ||||||
chr4:83443413
|
C | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1563+104G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443413 | ||||||
chr4:83443443
|
T | A | 1 | a0004c0010t0001g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1563+74A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443443 | ||||||
chr4:83443451
|
C | T | 12 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(9): Show | 14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563+66G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443451 | ||||||
chr4:83443655
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1466-41A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443655 | ||||||
chr4:83443684
|
T | C | 1 | a0001c0004t0001g0112 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1466-70A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443684 | ||||||
chr4:83443807
|
G | A | 7 | a0001c0004t0001g0021a0001c0004t0001g0118a0001c0004t0001g0120others(4): Show | 8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1466-193C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443807 | ||||||
chr4:83443871
|
C | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1466-257G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443871 | ||||||
chr4:83443959
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 125 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1466-345G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443959 | ||||||
chr4:83444052
|
G | A | 2 | a0001c0004t0001g0115a0002c0002t0001g0052 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1466-438C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444052 | ||||||
chr4:83444475
|
G | A | 1 | a0003c0003t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1466-861C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444475 | ||||||
chr4:83444491
|
CT | C | 153 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(150): Show | 184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1466-878delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444491 | ||||||
chr4:83444585
|
T | C | 27 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(24): Show | 30 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1466-971A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444585 | ||||||
chr4:83444652
|
T | C | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1466-1038A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444652 | ||||||
chr4:83444875
|
T | C | 6 | a0002c0002t0001g0086a0004c0005t0002g0032a0004c0005t0002g0257others(3): Show | 8 | HG01167.hp2 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1465+1139A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444875 | ||||||
chr4:83444998
|
G | A | 1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1465+1016C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444998 | ||||||
chr4:83445005
|
A | T | 1 | a0002c0002t0001g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1465+1009T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445005 | ||||||
chr4:83445144
|
C | T | 1 | a0010c0018t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1465+870G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445144 | ||||||
chr4:83445214
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 200 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.1465+800C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445214 | ||||||
chr4:83445257
|
A | T | 2 | a0001c0004t0001g0115a0002c0002t0001g0052 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1465+757T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445257 | ||||||
chr4:83445426
|
G | A | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1465+588C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445426 | ||||||
chr4:83445470
|
A | T | 15 | a0003c0015t0001g0103a0003c0016t0001g0105a0004c0005t0001g0019others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1465+544T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445470 | ||||||
chr4:83445584
|
T | C | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1465+430A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445584 | ||||||
chr4:83445602
|
A | G | 15 | a0003c0015t0001g0103a0003c0016t0001g0105a0004c0005t0001g0019others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1465+412T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445602 | ||||||
chr4:83445897
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1465+117C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445897 | ||||||
chr4:83446006
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02074.hp1 | splice_region_variant&intron_variant | LOW | c.1465+8T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83446006 | ||||||
chr4:83446133
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1393-47C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446133 | ||||||
chr4:83446139
|
A | G | 1 | a0002c0002t0001g0016 | 2 | HG01099.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1393-53T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446139 | ||||||
chr4:83446151
|
C | T | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0203others(1): Show | 4 | HG01255.hp2 HG01346.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1393-65G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446151 | ||||||
chr4:83446314
|
AT | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1393-229delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446314 | ||||||
chr4:83446315
|
T | A | 3 | a0002c0002t0001g0052a0008c0012t0001g0053a0008c0012t0001g0054 | 3 | HG01891.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1393-229A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446315 | ||||||
chr4:83446354
|
T | G | 12 | a0001c0004t0001g0021a0001c0004t0001g0115a0001c0004t0001g0116others(9): Show | 13 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.1393-268A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446354 | ||||||
chr4:83446368
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0209a0001c0001t0001g0213others(1): Show | 6 | HG00558.hp2 HG01952.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-282C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446368 | ||||||
chr4:83446451
|
C | T | 3 | a0003c0015t0001g0103a0003c0016t0001g0105a0004c0005t0001g0104 | 3 | HG02451.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1393-365G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446451 | ||||||
chr4:83446452
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1393-366C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446452 | ||||||
chr4:83446606
|
A | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1392+229T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446606 | ||||||
chr4:83446687
|
T | C | 4 | a0002c0002t0001g0077a0002c0002t0001g0078a0002c0002t0001g0079others(1): Show | 4 | HG00099.hp1 HG01256.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+148A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446687 | ||||||
chr4:83447072
|
GCATTGTG others(17): Show |
G | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1192-61_1192-38del others(24): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447072 | ||||||
chr4:83447077
|
G | T | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1192-42C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447077 | ||||||
chr4:83447477
|
G | A | 32 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(29): Show | 37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1192-442C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447477 | ||||||
chr4:83447496
|
C | G | 15 | a0003c0015t0001g0103a0003c0016t0001g0105a0004c0005t0001g0019others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192-461G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447496 | ||||||
chr4:83447761
|
G | A | 32 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(29): Show | 37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1192-726C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447761 | ||||||
chr4:83447859
|
C | CA | 17 | a0001c0001t0001g0179a0001c0001t0001g0198a0001c0001t0001g0199others(14): Show | 20 | HG00140.hp2 HG01243.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1192-825dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447859 | ||||||
chr4:83447859
|
C | CAAAA | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-828_1192-825d others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447859 | ||||||
chr4:83447884
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1192-849T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447884 | ||||||
chr4:83447931
|
C | T | 1 | a0001c0004t0001g0020 | 2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1191+852G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447931 | ||||||
chr4:83447964
|
C | T | 35 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(32): Show | 41 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1191+819G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447964 | ||||||
chr4:83447997
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+786C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447997 | ||||||
chr4:83448039
|
A | C | 1 | a0003c0003t0002g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1191+744T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448039 | ||||||
chr4:83448396
|
G | A | 1 | a0002c0002t0001g0012 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1191+387C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448396 | ||||||
chr4:83448441
|
G | A | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+342C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448441 | ||||||
chr4:83448489
|
G | A | 1 | a0002c0002t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1191+294C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448489 | ||||||
chr4:83448584
|
C | T | 1 | a0003c0003t0002g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1191+199G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448584 | ||||||
chr4:83448669
|
C | CA | 139 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 164 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.1191+113dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448669 | ||||||
chr4:83448670
|
A | AG | 2 | a0001c0001t0001g0008a0001c0001t0001g0220 | 4 | HG00741.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1191+112_1191+113i others(3): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448670 | ||||||
chr4:83448684
|
AG | A | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+98delC | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448684 | ||||||
chr4:83448971
|
TA | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1013-11delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83448971 | ||||||
chr4:83449154
|
C | T | 2 | a0003c0015t0001g0103a0003c0016t0001g0105 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1013-193G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449154 | ||||||
chr4:83449191
|
C | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1013-230G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449191 | ||||||
chr4:83449230
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(67): Show | 85 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1013-269A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449230 | ||||||
chr4:83449239
|
C | T | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1013-278G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449239 | ||||||
chr4:83449240
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1013-279C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449240 | ||||||
chr4:83449263
|
A | G | 2 | a0008c0012t0001g0053a0008c0012t0001g0054 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1013-302T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449263 | ||||||
chr4:83449297
|
G | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1013-336C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449297 | ||||||
chr4:83449306
|
C | T | 1 | a0002c0002t0001g0036 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1013-345G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449306 | ||||||
chr4:83449307
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(25): Show | 31 | HG00609.hp2 HG01109.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1013-346C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449307 | ||||||
chr4:83449307
|
G | T | 50 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(47): Show | 57 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.1013-346C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449307 | ||||||
chr4:83449350
|
C | T | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02056.hp2 HG02165.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-389G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449350 | ||||||
chr4:83449391
|
G | A | 2 | a0001c0001t0001g0144a0010c0018t0001g0143 | 2 | HG00280.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1013-430C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449391 | ||||||
chr4:83449736
|
G | GGCAAATG others(34): Show |
1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1013-816_1013-776d others(43): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449736 | ||||||
chr4:83449868
|
C | CA | 95 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(92): Show | 115 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1013-908dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449868 | ||||||
chr4:83449943
|
G | A | 25 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(22): Show | 28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1013-982C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449943 | ||||||
chr4:83449990
|
T | C | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-1029A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449990 | ||||||
chr4:83450006
|
A | C | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1045T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450006 | ||||||
chr4:83450007
|
C | T | 25 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(22): Show | 28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1013-1046G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450007 | ||||||
chr4:83450057
|
C | T | 1 | a0001c0006t0001g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1013-1096G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450057 | ||||||
chr4:83450128
|
C | T | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1167G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450128 | ||||||
chr4:83450203
|
T | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1242A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450203 | ||||||
chr4:83450218
|
A | G | 35 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(32): Show | 41 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1013-1257T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450218 | ||||||
chr4:83450222
|
T | TA | 13 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0019t0001g0157others(10): Show | 16 | HG01168.hp1 HG02109.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.1013-1262dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
T | TAA | 24 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0128others(21): Show | 27 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1013-1263_1013-126 others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
T | TAAA | 36 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(33): Show | 45 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1013-1264_1013-126 others(7): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
T | TAAAA | 30 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 36 | HG00408.hp2 HG00673.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1013-1265_1013-126 others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
T | TAAAAA | 12 | a0001c0001t0001g0026a0001c0001t0001g0200a0001c0001t0001g0201others(9): Show | 13 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1266_1013-126 others(9): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
T | TAAAAAA | 7 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0210others(4): Show | 10 | HG00558.hp2 HG01106.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-1267_1013-126 others(10): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
TAAA | T | 8 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(5): Show | 9 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-1264_1013-126 others(7): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
TAAAA | T | 9 | a0001c0004t0001g0021a0001c0004t0001g0115a0001c0004t0001g0116others(6): Show | 10 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1013-1265_1013-126 others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
TAAAAAAA others(3): Show |
T | 27 | a0003c0003t0002g0011a0003c0003t0002g0233a0003c0003t0002g0235others(24): Show | 31 | HG01109.hp1 HG01167.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1013-1271_1013-126 others(14): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
TAAAAAAA others(4): Show |
T | 3 | a0003c0003t0002g0030a0003c0003t0002g0234a0013c0013t0002g0255 | 4 | HG02055.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1272_1013-126 others(15): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
TAAAAAAA others(5): Show |
T | 1 | a0003c0016t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1013-1273_1013-126 others(16): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450222
|
TAAAAAAA others(7): Show |
T | 13 | a0002c0002t0001g0035a0004c0005t0001g0019a0004c0005t0001g0095others(10): Show | 14 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1013-1275_1013-126 others(18): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | ||||||
chr4:83450364
|
T | TA | 5 | a0003c0015t0001g0103a0003c0016t0001g0105a0004c0005t0002g0032others(2): Show | 6 | HG01167.hp2 HG02055.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-1404dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450364 | ||||||
chr4:83450542
|
C | T | 4 | a0001c0001t0001g0125a0005c0007t0001g0028a0005c0007t0001g0114others(1): Show | 5 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1581G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450542 | ||||||
chr4:83450664
|
C | CA | 9 | a0001c0001t0001g0215a0001c0001t0001g0216a0002c0002t0001g0015others(6): Show | 10 | HG03516.hp1 HG03704.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-1704dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450664 | ||||||
chr4:83450664
|
CA | C | 50 | a0001c0001t0001g0154a0002c0002t0001g0051a0002c0002t0001g0052others(47): Show | 57 | HG01167.hp2 HG01243.hp2 HG01891.hp1 others(54): Show |
intron_variant | MODIFIER | c.1013-1704delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450664 | ||||||
chr4:83450688
|
G | A | 2 | a0002c0002t0001g0089a0002c0002t0001g0090 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1013-1727C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450688 | ||||||
chr4:83450693
|
C | A | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1732G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450693 | ||||||
chr4:83450719
|
C | A | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-1758G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450719 | ||||||
chr4:83450773
|
C | G | 1 | a0003c0003t0002g0233 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1013-1812G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450773 | ||||||
chr4:83450792
|
C | A | 1 | a0003c0003t0002g0246 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1013-1831G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450792 | ||||||
chr4:83450871
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1013-1910A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450871 | ||||||
chr4:83450909
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1013-1948A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450909 | ||||||
chr4:83450999
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 134 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1013-2038T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450999 | ||||||
chr4:83451050
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1013-2089G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451050 | ||||||
chr4:83451106
|
T | C | 50 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(47): Show | 57 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.1012+2125A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451106 | ||||||
chr4:83451242
|
C | CA | 32 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(29): Show | 37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012+1988dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451242 | ||||||
chr4:83451286
|
A | C | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1012+1945T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451286 | ||||||
chr4:83451296
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1012+1935A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451296 | ||||||
chr4:83451324
|
G | A | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1012+1907C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451324 | ||||||
chr4:83451506
|
C | CA | 32 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(29): Show | 37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012+1724dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451506 | ||||||
chr4:83451523
|
G | A | 7 | a0003c0003t0002g0011a0003c0003t0002g0247a0003c0003t0002g0248others(4): Show | 9 | HG02258.hp2 HG02622.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+1708C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451523 | ||||||
chr4:83451553
|
C | T | 1 | a0004c0005t0001g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1012+1678G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451553 | ||||||
chr4:83451584
|
C | T | 3 | a0003c0015t0001g0103a0003c0016t0001g0105a0004c0005t0001g0104 | 3 | HG02451.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1012+1647G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451584 | ||||||
chr4:83451672
|
AC | A | 33 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(30): Show | 39 | HG01167.hp2 HG02145.hp2 HG02258.hp2 others(36): Show |
intron_variant | MODIFIER | c.1012+1558delG | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451672 | ||||||
chr4:83451673
|
C | A | 17 | a0003c0003t0002g0254a0003c0015t0001g0103a0004c0005t0001g0019others(14): Show | 18 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1012+1558G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451673 | ||||||
chr4:83451675
|
A | C | 3 | a0005c0007t0001g0028a0005c0007t0001g0114a0005c0007t0001g0223 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+1556T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451675 | ||||||
chr4:83451845
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 279 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1012+1386A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451845 | ||||||
chr4:83451994
|
G | A | 25 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(22): Show | 28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1012+1237C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451994 | ||||||
chr4:83452415
|
C | G | 2 | a0004c0011t0002g0231a0004c0011t0002g0232 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1012+816G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452415 | ||||||
chr4:83452457
|
G | A | 1 | a0001c0004t0001g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1012+774C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452457 | ||||||
chr4:83452469
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1012+762T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452469 | ||||||
chr4:83452473
|
G | A | 1 | a0003c0015t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1012+758C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452473 | ||||||
chr4:83452682
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1012+549C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452682 | ||||||
chr4:83452738
|
T | C | 1 | a0004c0005t0001g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1012+493A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452738 | ||||||
chr4:83452901
|
A | G | 1 | a0005c0007t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1012+330T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452901 | ||||||
chr4:83452966
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1012+265G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452966 | ||||||
chr4:83452974
|
TGAGGAAT others(2): Show |
T | 48 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(45): Show | 54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.1012+248_1012+256d others(11): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452974 | ||||||
chr4:83453076
|
G | A | 48 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(45): Show | 54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.1012+155C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83453076 | ||||||
chr4:83453964
|
C | T | 1 | a0002c0021t0001g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298-19G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83453964 | ||||||
chr4:83454033
|
G | T | 1 | a0005c0007t0001g0028 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.298-88C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454033 | ||||||
chr4:83454132
|
A | G | 9 | a0001c0004t0001g0020a0001c0004t0001g0106a0001c0004t0001g0107others(6): Show | 10 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-187T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454132 | ||||||
chr4:83454134
|
C | T | 12 | a0004c0005t0001g0019a0004c0005t0001g0095a0004c0005t0001g0096others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.298-189G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454134 | ||||||
chr4:83454136
|
C | G | 48 | a0003c0003t0002g0011a0003c0003t0002g0030a0003c0003t0002g0233others(45): Show | 54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.298-191G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454136 | ||||||
chr4:83454155
|
A | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0126others(27): Show | 33 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.298-210T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454155 | ||||||
chr4:83454196
|
C | G | 1 | a0004c0005t0002g0230 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.298-251G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454196 | ||||||
chr4:83454233
|
C | A | 1 | a0001c0001t0001g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.298-288G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454233 | ||||||
chr4:83454367
|
T | A | 4 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0093others(1): Show | 4 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-422A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454367 | ||||||
chr4:83454405
|
T | C | 5 | a0004c0005t0002g0032a0004c0005t0002g0257a0007c0009t0002g0031others(2): Show | 7 | HG01167.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-460A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454405 | ||||||
chr4:83454581
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.298-636C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454581 | ||||||
chr4:83454591
|
T | A | 1 | a0003c0003t0002g0258 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.298-646A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454591 | ||||||
chr4:83454644
|
C | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 134 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.298-699G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454644 | ||||||
chr4:83455086
|
T | A | 2 | a0005c0007t0001g0028a0005c0007t0001g0223 | 3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.297+311A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83455086 | ||||||
chr4:83455290
|
T | C | 34 | a0002c0002t0001g0029a0003c0003t0002g0011a0003c0003t0002g0030others(31): Show | 40 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+107A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83455290 |