geneid | 3162 |
---|---|
ensemblid | ENSG00000100292.18 |
hgncid | 5013 |
symbol | HMOX1 |
name | heme oxygenase 1 |
refseq_nuc | NM_002133.3 |
refseq_prot | NP_002124.1 |
ensembl_nuc | ENST00000216117.9 |
ensembl_prot | ENSP00000216117.8 |
mane_status | MANE Select |
chr | chr22 |
start | 35381096 |
end | 35394207 |
strand | + |
ver | v1.2 |
region | chr22:35381096-35394207 |
region5000 | chr22:35376096-35399207 |
regionname0 | HMOX1_chr22_35381096_35394207 |
regionname5000 | HMOX1_chr22_35376096_35399207 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 288 | 362 | 76 | 62 | 167 | 16 | 39 | 128 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0002 | 0/0 | 288 | 17 | 3 | 0 | 14 | 0 | 0 | 11 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0003 | 0/0 | 288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0004 | 0/0 | 288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0005 | 0/0 | 288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0006 | 0/0 | 288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0007 | 0/0 | 288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 867 | 354 | 68 | 62 | 167 | 16 | 39 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0002 | 0/0 | 867 | 17 | 3 | 0 | 14 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0003 | 0/0 | 867 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0004 | 0/0 | 867 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0005 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0006 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0007 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0008 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0009 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0010 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
c0011 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 688 | 337 | 41 | 60 | 179 | 16 | 39 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0002 | 0/0 | 688 | 29 | 28 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0003 | 0/0 | 688 | 5 | 5 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0004 | 0/0 | 696 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0005 | 0/0 | 688 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0006 | 0/0 | 696 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0007 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0008 | 0/0 | 688 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0009 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0010 | 0/0 | 688 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0011 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
t0012 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 6 | 0 | 3 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0002 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0007 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 867 | 354 | 68 | 62 | 167 | 16 | 39 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0003 | 0/0 | 867 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0004 | 0/0 | 867 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0006 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0011 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0002c0002 | 0/0 | 867 | 17 | 3 | 0 | 14 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0003c0009 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0004c0007 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0005c0008 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0006c0010 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0007c0005 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1554 | 315 | 36 | 60 | 163 | 16 | 38 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0002 | 0/0 | 1554 | 24 | 23 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0003 | 0/0 | 1554 | 5 | 5 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0004 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0005 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0006 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0007 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0008 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0009 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0010 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0001t0012 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0003t0001 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0003t0002 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0004t0004 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0006t0002 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0001c0011t0001 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0002c0002t0001 | 0/0 | 1554 | 15 | 1 | 0 | 14 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0002c0002t0002 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0003c0009t0001 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0004c0007t0011 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0005c0008t0001 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0006c0010t0001 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
a0007c0005t0001 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | copy fasta | chr22 | 35376096 | 35399207 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 6 | 0 | 3 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0007 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0008g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0010g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0001t0012g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0003t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0004t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0004t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0006t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0001c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0002c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0003c0009t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0004c0007t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0005c0008t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0006c0010t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
a0007c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01496 | hp1 | a0001 | c0001 | t0010 | g0182 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02257 | hp1 | a0001 | c0011 | t0001 | g0041 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02630 | hp1 | a0001 | c0004 | t0004 | g0196 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0183 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02717 | hp1 | a0005 | c0008 | t0001 | g0345 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02818 | hp1 | a0001 | c0004 | t0004 | g0195 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02897 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0298 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0299 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03710 | hp2 | a0003 | c0009 | t0001 | g0023 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0242 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18969 | hp1 | a0007 | c0005 | t0001 | g0326 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18986 | hp1 | a0004 | c0007 | t0011 | g0100 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19009 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19079 | hp1 | a0006 | c0010 | t0001 | g0294 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20129 | hp1 | a0001 | c0006 | t0002 | g0350 | AFR | ASW | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | GIH | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0270 | REF | REF | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35381192
|
G | C | 1 | a0002 | 17 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(14): Show |
missense_variant | MODERATE | c.19G>C | p.Asp7His | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/5 | 97/1554 | 19/867 | 7/288 | chr22 | 35381192 | ||
chr22:35383131
|
C | A | 1 | a0007 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.49C>A | p.Leu17Met | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/5 | 127/1554 | 49/867 | 17/288 | chr22 | 35383131 | ||
chr22:35386997
|
A | C | 1 | a0006 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.457A>C | p.Lys153Gln | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 535/1554 | 457/867 | 153/288 | chr22 | 35386997 | ||
chr22:35386998
|
A | T | 1 | a0006 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.458A>T | p.Lys153Ile | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 536/1554 | 458/867 | 153/288 | chr22 | 35386998 | ||
chr22:35386999
|
A | C | 1 | a0006 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.459A>C | p.Lys153Asn | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 537/1554 | 459/867 | 153/288 | chr22 | 35386999 | ||
chr22:35387156
|
G | T | 1 | a0007 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.616G>T | p.Ala206Ser | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 694/1554 | 616/867 | 206/288 | chr22 | 35387156 | ||
chr22:35389903
|
A | G | 1 | a0003 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.676A>G | p.Lys226Glu | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/5 | 754/1554 | 676/867 | 226/288 | chr22 | 35389903 | ||
chr22:35393479
|
G | C | 1 | a0004 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.748G>C | p.Val250Leu | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 826/1554 | 748/867 | 250/288 | chr22 | 35393479 | ||
chr22:35393480
|
T | G | 1 | a0004 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.749T>G | p.Val250Gly | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 827/1554 | 749/867 | 250/288 | chr22 | 35393480 | ||
chr22:35393483
|
A | T | 1 | a0004 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.752A>T | p.Glu251Val | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 830/1554 | 752/867 | 251/288 | chr22 | 35393483 | ||
chr22:35393567
|
C | T | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.836C>T | p.Ala279Val | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 914/1554 | 836/867 | 279/288 | chr22 | 35393567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35386918
|
C | T | 1 | a0001c0011 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.378C>T | p.Pro126Pro | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 456/1554 | 378/867 | 126/288 | chr22 | 35386918 | ||
chr22:35387143
|
A | G | 1 | a0001c0003 | 4 | HG02055.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
synonymous_variant | LOW | c.603A>G | p.Glu201Glu | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 681/1554 | 603/867 | 201/288 | chr22 | 35387143 | ||
chr22:35387158
|
G | A | 1 | a0001c0006 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.618G>A | p.Ala206Ala | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 696/1554 | 618/867 | 206/288 | chr22 | 35387158 | ||
chr22:35393481
|
G | T | 1 | a0004c0007 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.750G>T | p.Val250Val | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 828/1554 | 750/867 | 250/288 | chr22 | 35393481 | ||
chr22:35393571
|
A | G | 1 | a0001c0004 | 2 | HG02630.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.840A>G | p.Thr280Thr | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 918/1554 | 840/867 | 280/288 | chr22 | 35393571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35381102
|
T | G | 1 | a0001c0001t0006 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/5 | 72 | chr22 | 35381102 | |||||
chr22:35381137
|
C | G | 1 | a0001c0001t0012 | 1 | NA19009.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/5 | 37 | chr22 | 35381137 | |||||
chr22:35393662
|
G | C | 1 | a0001c0001t0005 | 2 | NA18963.hp1 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*64G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 64 | chr22 | 35393662 | |||||
chr22:35393692
|
G | T | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 94 | chr22 | 35393692 | |||||
chr22:35393701
|
A | C | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 103 | chr22 | 35393701 | |||||
chr22:35393732
|
G | T | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 134 | chr22 | 35393732 | |||||
chr22:35393733
|
T | C | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 135 | chr22 | 35393733 | |||||
chr22:35393842
|
C | T | 3 | a0001c0001t0003a0001c0001t0009a0001c0001t0010 | 7 | HG01496.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 244 | chr22 | 35393842 | |||||
chr22:35393876
|
A | G | 5 | a0001c0001t0002a0001c0001t0003a0001c0003t0002others(2): Show | 34 | HG01192.hp2 HG02055.hp1 HG02258.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*278A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 278 | chr22 | 35393876 | |||||
chr22:35393915
|
C | T | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*317C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 317 | chr22 | 35393915 | |||||
chr22:35393916
|
T | G | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*318T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 318 | chr22 | 35393916 | |||||
chr22:35393917
|
G | A | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*319G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 319 | chr22 | 35393917 | |||||
chr22:35393978
|
T | G | 1 | a0001c0001t0007 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 380 | chr22 | 35393978 | |||||
chr22:35394089
|
T | A | 1 | a0004c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 491 | chr22 | 35394089 | |||||
chr22:35394154
|
T | TTAAAGTT others(1): Show |
3 | a0001c0001t0004a0001c0001t0006a0001c0004t0004 | 5 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*556_*557insTAAAGT others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 557 | chr22 | 35394154 | |||||
chr22:35394181
|
A | G | 1 | a0001c0001t0008 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 583 | chr22 | 35394181 | |||||
chr22:35394202
|
A | T | 1 | a0001c0001t0010 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 604 | chr22 | 35394202 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35381210
|
G | A | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.23+14G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381210 | ||||||
chr22:35381230
|
C | G | 1 | a0001c0006t0002g0350 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.23+34C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381230 | ||||||
chr22:35381268
|
C | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | NA18947.hp2 NA19062.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.23+72C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381268 | ||||||
chr22:35381301
|
G | C | 1 | a0001c0001t0012g0024 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.23+105G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381301 | ||||||
chr22:35381302
|
C | G | 1 | a0001c0001t0012g0024 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.23+106C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381302 | ||||||
chr22:35381357
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.23+161C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381357 | ||||||
chr22:35381358
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027 | 4 | HG00408.hp1 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+162G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381358 | ||||||
chr22:35381466
|
A | AT | 7 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0342others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+280dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35381466 | |||||
chr22:35381466
|
A | T | 1 | a0001c0001t0001g0346 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.23+270A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381466 | ||||||
chr22:35381569
|
G | GGTGGCAT others(113): Show |
1 | a0001c0001t0001g0025 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.23+375_23+494dupTG others(118): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35381569 | |||||
chr22:35381579
|
G | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01192.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+383G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381579 | ||||||
chr22:35381625
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.23+429G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381625 | ||||||
chr22:35381772
|
A | AT | 36 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0310others(33): Show | 36 | HG00408.hp2 HG01081.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.23+587dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35381772 | |||||
chr22:35381863
|
C | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(58): Show | 65 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.23+667C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381863 | ||||||
chr22:35381910
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG00099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.23+714G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381910 | ||||||
chr22:35381957
|
G | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+761G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381957 | ||||||
chr22:35381991
|
A | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.23+795A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381991 | ||||||
chr22:35382007
|
C | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+811C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382007 | ||||||
chr22:35382164
|
T | C | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.24-942T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382164 | ||||||
chr22:35382184
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.24-922C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382184 | ||||||
chr22:35382201
|
C | G | 1 | a0001c0006t0002g0350 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.24-905C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382201 | ||||||
chr22:35382269
|
T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-837T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382269 | ||||||
chr22:35382285
|
A | G | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(57): Show | 64 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.24-821A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382285 | ||||||
chr22:35382372
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.24-734G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382372 | ||||||
chr22:35382395
|
A | G | 1 | a0001c0001t0006g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.24-711A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382395 | ||||||
chr22:35382413
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.24-693G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382413 | ||||||
chr22:35382497
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.24-609G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382497 | ||||||
chr22:35382512
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(175): Show | 189 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.24-594C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382512 | ||||||
chr22:35382517
|
A | AT | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0019others(59): Show | 67 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.24-572dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382517 | |||||
chr22:35382517
|
A | ATT | 10 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 11 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.24-573_24-572dupTT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382517 | |||||
chr22:35382517
|
AT | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0188a0001c0001t0001g0189others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.24-572delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382517 | |||||
chr22:35382535
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-571G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382535 | ||||||
chr22:35382609
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-497C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382609 | ||||||
chr22:35382663
|
C | CT | 130 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(127): Show | 139 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.24-436dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382663 | |||||
chr22:35382663
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.24-443C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382663 | ||||||
chr22:35382671
|
C | CT | 7 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(4): Show | 7 | HG01192.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.24-426dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382671 | |||||
chr22:35382671
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0006g0183 | 2 | HG02647.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.24-435C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382671 | ||||||
chr22:35382734
|
T | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(56): Show | 63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.24-372T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382734 | ||||||
chr22:35382760
|
C | G | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(57): Show | 64 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.24-346C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382760 | ||||||
chr22:35382846
|
C | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(42): Show | 48 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.24-260C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382846 | ||||||
chr22:35382872
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0002g0191 | 3 | HG03516.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.24-234G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382872 | ||||||
chr22:35382968
|
A | C | 13 | a0002c0002t0001g0021a0002c0002t0001g0300a0002c0002t0001g0301others(10): Show | 14 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.24-138A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382968 | ||||||
chr22:35383230
|
T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.144+4T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383230 | ||||||
chr22:35383261
|
G | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0346 | 2 | HG00597.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.144+35G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383261 | ||||||
chr22:35383323
|
C | T | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.144+97C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383323 | ||||||
chr22:35383438
|
A | AAAAAAAG others(31): Show |
1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+212_144+213ins others(38): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383438 | ||||||
chr22:35383443
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+217C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383443 | ||||||
chr22:35383444
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+218T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383444 | ||||||
chr22:35383449
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+223C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383449 | ||||||
chr22:35383451
|
GCAGTGCC others(65): Show |
G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+227_144+298del others(72): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35383451 | |||||
chr22:35383492
|
T | G | 1 | a0001c0001t0006g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.144+266T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383492 | ||||||
chr22:35383524
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+298C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383524 | ||||||
chr22:35383525
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+299T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383525 | ||||||
chr22:35383528
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+302C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383528 | ||||||
chr22:35383529
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+303G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383529 | ||||||
chr22:35383535
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+309G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383535 | ||||||
chr22:35383537
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+311T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383537 | ||||||
chr22:35383538
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+312G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383538 | ||||||
chr22:35383539
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+313A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383539 | ||||||
chr22:35383540
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+314G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383540 | ||||||
chr22:35383548
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+322A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383548 | ||||||
chr22:35383549
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+323G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383549 | ||||||
chr22:35383551
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+325C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383551 | ||||||
chr22:35383575
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(55): Show | 62 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.144+349G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383575 | ||||||
chr22:35383622
|
C | T | 1 | a0002c0002t0001g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.144+396C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383622 | ||||||
chr22:35383637
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.144+411A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383637 | ||||||
chr22:35383642
|
T | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0002g0045others(13): Show | 17 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.144+416T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383642 | ||||||
chr22:35383655
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0181 | 2 | NA18950.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.144+429C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383655 | ||||||
chr22:35383851
|
T | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(43): Show | 49 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.144+625T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383851 | ||||||
chr22:35383914
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.144+688C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383914 | ||||||
chr22:35383951
|
AAGAGCTT others(39): Show |
A | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.144+728_144+773del others(46): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35383951 | |||||
chr22:35383981
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.144+755G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383981 | ||||||
chr22:35384024
|
G | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.144+798G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384024 | ||||||
chr22:35384056
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.144+830C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384056 | ||||||
chr22:35384192
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG00733.hp1 HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.144+966C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384192 | ||||||
chr22:35384284
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.144+1058A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384284 | ||||||
chr22:35384371
|
AC | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01192.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+1147delC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35384371 | |||||
chr22:35384701
|
T | A | 1 | a0001c0001t0001g0347 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.144+1475T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384701 | ||||||
chr22:35385122
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.145-1563C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385122 | ||||||
chr22:35385213
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.145-1472G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385213 | ||||||
chr22:35385214
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.145-1471T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385214 | ||||||
chr22:35385221
|
C | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(55): Show | 62 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.145-1464C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385221 | ||||||
chr22:35385227
|
G | A | 2 | a0001c0004t0004g0195a0001c0004t0004g0196 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.145-1458G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385227 | ||||||
chr22:35385271
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.145-1414C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385271 | ||||||
chr22:35385433
|
A | AT | 71 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0025others(68): Show | 74 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.145-1234dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385433 | |||||
chr22:35385433
|
A | ATT | 8 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 9 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-1235_145-1234d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385433 | |||||
chr22:35385433
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.145-1247_145-1234d others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385433 | |||||
chr22:35385574
|
GGACTATA others(60): Show |
G | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.145-1109_145-1043d others(69): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385574 | |||||
chr22:35385609
|
C | CT | 42 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0260others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.145-1054dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385609 | |||||
chr22:35385609
|
CT | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.145-1054delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385609 | |||||
chr22:35385609
|
CTT | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(46): Show | 52 | HG00408.hp1 HG00597.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.145-1055_145-1054d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385609 | |||||
chr22:35385617
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.145-1058_145-1057i others(13): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385617 | |||||
chr22:35385673
|
T | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 8 | NA18948.hp1 NA18967.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.145-1012T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385673 | ||||||
chr22:35385936
|
G | GTTTA | 14 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.145-729_145-726dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385936 | |||||
chr22:35386017
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.145-668G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386017 | ||||||
chr22:35386056
|
C | T | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145-629C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386056 | ||||||
chr22:35386149
|
G | C | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145-536G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386149 | ||||||
chr22:35386339
|
T | TTAAGCAA others(31): Show |
1 | a0001c0001t0001g0164 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.145-345_145-308dup others(38): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35386339 | |||||
chr22:35386380
|
TACAGGGG others(15): Show |
T | 1 | a0001c0001t0001g0152 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.145-304_145-283del others(22): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386380 | ||||||
chr22:35386494
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.145-191T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386494 | ||||||
chr22:35386515
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.145-170A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386515 | ||||||
chr22:35386520
|
C | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(43): Show | 49 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.145-165C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386520 | ||||||
chr22:35386666
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-19C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386666 | ||||||
chr22:35387293
|
C | T | 7 | a0001c0001t0001g0325a0001c0001t0002g0028a0001c0001t0002g0029others(4): Show | 7 | HG01192.hp2 HG02056.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+117C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387293 | ||||||
chr22:35387371
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.636+195A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387371 | ||||||
chr22:35387410
|
G | A | 1 | a0007c0005t0001g0326 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.636+234G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387410 | ||||||
chr22:35387420
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(246): Show | 263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.636+244A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387420 | ||||||
chr22:35387558
|
C | T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.636+382C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387558 | ||||||
chr22:35387559
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.636+383A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387559 | ||||||
chr22:35387592
|
T | TACAGGTG others(65): Show |
1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.636+418_636+489dup others(72): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35387592 | |||||
chr22:35387624
|
G | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(56): Show | 63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.636+448G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387624 | ||||||
chr22:35387626
|
CTAGCCAG others(25): Show |
C | 1 | a0001c0001t0001g0295 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.636+452_636+483del others(32): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35387626 | |||||
chr22:35387721
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.636+545G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387721 | ||||||
chr22:35387783
|
C | T | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01192.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+607C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387783 | ||||||
chr22:35387853
|
A | C | 1 | a0001c0001t0004g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+677A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387853 | ||||||
chr22:35388002
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0201a0001c0001t0001g0202others(5): Show | 8 | NA18968.hp2 NA18972.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+826G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388002 | ||||||
chr22:35388030
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.636+854G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388030 | ||||||
chr22:35388042
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.636+866T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388042 | ||||||
chr22:35388061
|
T | G | 2 | a0002c0002t0002g0298a0002c0002t0002g0299 | 2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.636+885T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388061 | ||||||
chr22:35388096
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.636+920T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388096 | ||||||
chr22:35388107
|
TA | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0324a0001c0001t0001g0335 | 3 | NA18956.hp1 NA19012.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.636+937delA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388107 | |||||
chr22:35388126
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.636+950T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388126 | ||||||
chr22:35388131
|
G | GA | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(59): Show | 66 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.636+962dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388131 | |||||
chr22:35388287
|
C | CA | 13 | a0002c0002t0001g0021a0002c0002t0001g0300a0002c0002t0001g0301others(10): Show | 14 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.636+1116dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388287 | |||||
chr22:35388324
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.636+1148C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388324 | ||||||
chr22:35388394
|
G | A | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.636+1218G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388394 | ||||||
chr22:35388415
|
G | A | 3 | a0002c0002t0001g0208a0002c0002t0001g0263a0002c0002t0001g0264 | 3 | NA18975.hp2 NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.636+1239G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388415 | ||||||
chr22:35388466
|
AAAAAAC | A | 7 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(4): Show | 7 | HG01192.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+1308_636+1313d others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388466 | |||||
chr22:35388484
|
C | CA | 17 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0085others(14): Show | 17 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.636+1317dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388484 | |||||
chr22:35388510
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.636+1334G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388510 | ||||||
chr22:35388525
|
C | T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-1339C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388525 | ||||||
chr22:35388553
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.637-1311C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388553 | ||||||
chr22:35388554
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.637-1310G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388554 | ||||||
chr22:35388562
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-1302T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388562 | ||||||
chr22:35388614
|
C | A | 1 | a0001c0001t0001g0335 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.637-1250C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388614 | ||||||
chr22:35388624
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-1240A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388624 | ||||||
chr22:35388752
|
G | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(42): Show | 48 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.637-1112G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388752 | ||||||
chr22:35388754
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG01109.hp2 HG02922.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1110G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388754 | ||||||
chr22:35388763
|
C | T | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-1101C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388763 | ||||||
chr22:35388802
|
C | CA | 3 | a0001c0001t0001g0022a0001c0001t0001g0343a0001c0001t0001g0344 | 4 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-1056dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388802 | |||||
chr22:35388809
|
C | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-1055C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388809 | ||||||
chr22:35388809
|
C | CA | 22 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0035others(19): Show | 24 | HG00597.hp1 HG01168.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.637-1052dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388809 | |||||
chr22:35388809
|
C | CAA | 15 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0043others(12): Show | 16 | HG00408.hp1 HG02486.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-1053_637-1052d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388809 | |||||
chr22:35388812
|
A | AAC | 7 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(4): Show | 7 | HG01192.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1052_637-1051i others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388812 | ||||||
chr22:35388813
|
C | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(56): Show | 63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.637-1051C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388813 | ||||||
chr22:35388813
|
C | CA | 10 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0197others(7): Show | 10 | HG00621.hp2 HG01106.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.637-1042dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388813 | |||||
chr22:35388990
|
A | G | 2 | a0001c0001t0005g0093a0001c0001t0005g0148 | 2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.637-874A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388990 | ||||||
chr22:35388996
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.637-868T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388996 | ||||||
chr22:35389005
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(51): Show | 57 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.637-859A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389005 | ||||||
chr22:35389113
|
G | A | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-751G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389113 | ||||||
chr22:35389140
|
A | G | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-724A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389140 | ||||||
chr22:35389141
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027others(12): Show | 16 | HG00408.hp1 HG00597.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-723T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389141 | ||||||
chr22:35389189
|
T | TTTTC | 33 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(30): Show | 33 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.637-653_637-650dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | |||||
chr22:35389189
|
T | TTTTCTTT others(1): Show |
30 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(27): Show | 35 | HG00733.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.637-657_637-650dup others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | |||||
chr22:35389189
|
T | TTTTCTTT others(5): Show |
23 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0001g0081others(20): Show | 24 | HG01069.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.637-661_637-650dup others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | |||||
chr22:35389189
|
T | TTTTCTTT others(9): Show |
8 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG00558.hp2 HG01070.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-665_637-650dup others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | |||||
chr22:35389189
|
T | TTTTCTTT others(13): Show |
3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0157 | 3 | HG00438.hp1 NA18957.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.637-669_637-650dup others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | |||||
chr22:35389211
|
TTCTC | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0146others(1): Show | 5 | NA19011.hp1 NA19074.hp1 NA20752.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-649_637-646del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389211 | |||||
chr22:35389215
|
C | CTCTT | 27 | a0001c0001t0001g0025a0001c0001t0001g0188a0001c0001t0001g0189others(24): Show | 28 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.637-627_637-624dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389215 | |||||
chr22:35389215
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(170): Show | 183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.637-649C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389215 | ||||||
chr22:35389215
|
CTCTT | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0207a0001c0001t0001g0240others(13): Show | 17 | HG00140.hp1 HG00642.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.637-627_637-624del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389215 | |||||
chr22:35389223
|
TTCTTTC | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-639_637-634del others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389223 | |||||
chr22:35389229
|
C | CTTTCTT | 3 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | HG01168.hp2 HG01169.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.637-633_637-628dup others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(3): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-622_637-613dup others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(7): Show |
21 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0043others(18): Show | 21 | HG00408.hp1 HG02486.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.637-624_637-623ins others(14): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(10): Show |
1 | a0001c0001t0002g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.637-624_637-623ins others(17): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(11): Show |
9 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0055others(6): Show | 12 | HG00597.hp1 HG02135.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-624_637-623ins others(18): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(23): Show |
1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-624_637-623ins others(30): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(16): Show |
2 | a0001c0001t0002g0028a0001c0001t0002g0033 | 2 | HG01192.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.637-624_637-623ins others(23): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(12): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0032 | 3 | HG02258.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-624_637-623ins others(19): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389229
|
C | CTTTCTTT others(8): Show |
1 | a0001c0001t0002g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-623_637-622ins others(15): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | |||||
chr22:35389237
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637-627C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389237 | ||||||
chr22:35389238
|
T | TTTCTTTC others(8): Show |
1 | a0001c0001t0001g0088 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.637-624_637-623ins others(15): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389238 | |||||
chr22:35389239
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637-625T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389239 | ||||||
chr22:35389239
|
T | TTC | 4 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0010g0182others(1): Show | 4 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-624_637-623ins others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389239 | |||||
chr22:35389239
|
T | TTCTTTCT others(3): Show |
1 | a0001c0004t0004g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637-624_637-623ins others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389239 | |||||
chr22:35389241
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0347others(1): Show | 4 | HG02738.hp2 NA18963.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-623T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389241 | ||||||
chr22:35389243
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0347others(1): Show | 4 | HG02738.hp2 NA18963.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-621C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389243 | ||||||
chr22:35389250
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0010g0182 | 2 | HG01496.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.637-614T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389250 | ||||||
chr22:35389250
|
T | TC | 4 | a0001c0001t0001g0150a0001c0001t0001g0202a0001c0001t0001g0213others(1): Show | 4 | HG02738.hp2 NA18612.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-614_637-613ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389250 | ||||||
chr22:35389250
|
T | TTC | 13 | a0001c0001t0001g0018a0001c0001t0001g0235a0001c0001t0001g0236others(10): Show | 14 | HG00642.hp1 HG01109.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-591_637-590dup others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | |||||
chr22:35389250
|
TTC | T | 4 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0327others(1): Show | 4 | HG03831.hp2 NA18944.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-591_637-590del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | |||||
chr22:35389250
|
TTCTC | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0074others(11): Show | 16 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-593_637-590del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | |||||
chr22:35389250
|
TTCTCTCT others(7): Show |
T | 1 | a0001c0001t0001g0340 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.637-603_637-590del others(14): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | |||||
chr22:35389251
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.637-613T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389251 | ||||||
chr22:35389252
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0155a0001c0001t0001g0180others(1): Show | 4 | HG02738.hp1 HG02818.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-612C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389252 | ||||||
chr22:35389253
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-611T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389253 | ||||||
chr22:35389254
|
C | T | 6 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0085others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-610C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389254 | ||||||
chr22:35389256
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-608C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389256 | ||||||
chr22:35389258
|
C | T | 2 | a0001c0001t0001g0067a0001c0003t0001g0069 | 2 | HG02055.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.637-606C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389258 | ||||||
chr22:35389260
|
C | T | 2 | a0001c0001t0001g0064a0001c0003t0001g0069 | 2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.637-604C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389260 | ||||||
chr22:35389264
|
C | T | 2 | a0001c0001t0001g0064a0001c0003t0001g0069 | 2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.637-600C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389264 | ||||||
chr22:35389265
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-599T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389265 | ||||||
chr22:35389266
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-598C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389266 | ||||||
chr22:35389268
|
CT | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0177a0001c0001t0001g0346 | 3 | HG00597.hp2 NA18948.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.637-595delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389268 | ||||||
chr22:35389269
|
T | TC | 97 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.637-594dupC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389269 | |||||
chr22:35389270
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-594C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389270 | ||||||
chr22:35389271
|
TCTC | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(17): Show | 23 | HG00597.hp1 HG02135.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.637-589_637-587del others(3): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389271 | |||||
chr22:35389273
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0145a0001c0001t0001g0150 | 3 | HG01358.hp2 HG02738.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.637-591T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389273 | ||||||
chr22:35389273
|
TC | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 119 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.637-589delC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389273 | |||||
chr22:35389274
|
C | CT | 18 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0067others(15): Show | 18 | HG02055.hp1 HG02055.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.637-590_637-589ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389274 | ||||||
chr22:35389274
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0080a0001c0001t0001g0145others(1): Show | 4 | HG01243.hp2 HG01358.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-590C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389274 | ||||||
chr22:35389275
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0218others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-589C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389275 | ||||||
chr22:35389276
|
T | A | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.637-588T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389276 | ||||||
chr22:35389276
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0218a0001c0001t0001g0342others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-588T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389276 | ||||||
chr22:35389281
|
CTCTCTCT others(51): Show |
C | 2 | a0001c0001t0001g0022a0001c0001t0001g0342 | 3 | HG01070.hp2 HG01071.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.637-578_637-521del others(58): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389281 | |||||
chr22:35389282
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-582T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389282 | ||||||
chr22:35389284
|
T | TC | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0032 | 3 | HG02258.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-579dupC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389284 | |||||
chr22:35389285
|
CTCTCTTC others(29): Show |
C | 1 | a0001c0001t0001g0344 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637-578_637-543del others(36): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389285 | ||||||
chr22:35389285
|
CTCTCTTC others(37): Show |
C | 1 | a0005c0008t0001g0345 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.637-578_637-535del others(44): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389285 | ||||||
chr22:35389286
|
TCTC | T | 5 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0278others(2): Show | 5 | HG00438.hp2 NA18949.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-577_637-575del others(3): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389286 | ||||||
chr22:35389287
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 104 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.637-577C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389287 | ||||||
chr22:35389288
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.637-576T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389288 | ||||||
chr22:35389288
|
TCTTCTTT others(46): Show |
T | 1 | a0001c0001t0001g0343 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.637-575_637-523del others(53): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389288 | ||||||
chr22:35389289
|
C | CT | 3 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0006g0183 | 3 | HG01891.hp1 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.637-573dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | |||||
chr22:35389289
|
C | CTTCT | 6 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0150others(3): Show | 6 | HG02135.hp1 HG02738.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-569_637-566dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | |||||
chr22:35389289
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 104 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.637-575C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389289 | ||||||
chr22:35389289
|
CT | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-573delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | |||||
chr22:35389289
|
CTTCTTTC others(5): Show |
C | 1 | a0001c0001t0002g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637-573_637-562del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | |||||
chr22:35389290
|
T | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(29): Show | 35 | HG00408.hp1 HG00597.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.637-574T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389290 | ||||||
chr22:35389290
|
T | TC | 7 | a0001c0001t0001g0037a0001c0001t0002g0028a0001c0001t0002g0029others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-574_637-573ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389290 | ||||||
chr22:35389291
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0012g0024 | 2 | HG04228.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.637-573T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389291 | ||||||
chr22:35389294
|
T | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(48): Show | 54 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-570T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389294 | ||||||
chr22:35389295
|
T | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0218a0001c0001t0010g0182 | 3 | HG01496.hp1 NA18940.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.637-569T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389295 | ||||||
chr22:35389296
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0002g0033 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.637-567_637-566ins others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389296 | |||||
chr22:35389296
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0218a0001c0001t0002g0028 | 3 | HG02809.hp1 NA18940.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.637-568C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389296 | ||||||
chr22:35389296
|
CT | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(29): Show | 35 | HG00408.hp1 HG00597.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.637-566delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389296 | |||||
chr22:35389296
|
CTTCT | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0243a0001c0001t0001g0280 | 3 | HG01517.hp2 HG03041.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.637-546_637-543del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389296 | |||||
chr22:35389297
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0010g0182 | 3 | HG01496.hp1 HG04228.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.637-567T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389297 | ||||||
chr22:35389297
|
T | TC | 5 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0002g0048others(2): Show | 5 | HG02818.hp2 HG02886.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-567_637-566ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389297 | ||||||
chr22:35389298
|
T | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-566T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389298 | ||||||
chr22:35389299
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0099others(7): Show | 12 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-565C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389299 | ||||||
chr22:35389300
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0099others(4): Show | 9 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-564T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389300 | ||||||
chr22:35389301
|
T | C | 42 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(39): Show | 45 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.637-563T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389301 | ||||||
chr22:35389302
|
T | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-562T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389302 | ||||||
chr22:35389305
|
T | C | 42 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(39): Show | 45 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.637-559T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389305 | ||||||
chr22:35389305
|
TTC | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0211a0001c0001t0001g0231others(3): Show | 7 | HG00323.hp1 HG01081.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-557_637-556del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389305 | |||||
chr22:35389306
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-558T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389306 | ||||||
chr22:35389306
|
TCTTTCTT others(82): Show |
T | 3 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038 | 3 | HG01884.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.637-542_637-454del others(89): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389306 | |||||
chr22:35389309
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(38): Show | 44 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.637-555T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389309 | ||||||
chr22:35389310
|
TCTTTCTT others(78): Show |
T | 2 | a0001c0001t0001g0035a0001c0001t0001g0039 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.637-542_637-458del others(85): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389310 | |||||
chr22:35389311
|
CTTTCTTT others(89): Show |
C | 1 | a0001c0001t0002g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637-552_637-457del others(96): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389311 | ||||||
chr22:35389312
|
T | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-552T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389312 | ||||||
chr22:35389313
|
T | C | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(37): Show | 43 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.637-551T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389313 | ||||||
chr22:35389314
|
TCTTTCTT others(74): Show |
T | 1 | a0001c0001t0001g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.637-542_637-462del others(81): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389314 | |||||
chr22:35389315
|
CTTTCTTC others(97): Show |
C | 1 | a0001c0001t0002g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.637-548_637-445del | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389315 | ||||||
chr22:35389316
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-548T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389316 | ||||||
chr22:35389317
|
T | C | 39 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(36): Show | 42 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.637-547T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389317 | ||||||
chr22:35389318
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0281 | 2 | HG01516.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.637-546T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389318 | ||||||
chr22:35389318
|
TCTTCTTT others(70): Show |
T | 1 | a0001c0001t0002g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-542_637-466del others(77): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389318 | |||||
chr22:35389319
|
C | CT | 5 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0099others(2): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-543dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389319 | |||||
chr22:35389319
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0281 | 2 | HG01516.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.637-545C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | ||||||
chr22:35389319
|
CT | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG02135.hp2 HG03927.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-543delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389319 | |||||
chr22:35389319
|
CTTCTTTC others(77): Show |
C | 4 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0056others(1): Show | 4 | HG00408.hp1 HG03490.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-544_637-461del others(84): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | ||||||
chr22:35389319
|
CTTCTTTC others(79): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.637-523_637-438del others(86): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389319 | |||||
chr22:35389319
|
CTTCTTTC others(85): Show |
C | 3 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0070 | 4 | HG00597.hp1 NA18941.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-544_637-453del others(92): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | ||||||
chr22:35389319
|
CTTCTTTC others(89): Show |
C | 5 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG03139.hp2 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-544_637-449del others(96): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | ||||||
chr22:35389319
|
CTTCTTTC others(93): Show |
C | 7 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0002g0045others(4): Show | 8 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-544_637-445del others(100): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | ||||||
chr22:35389319
|
CTTCTTTC others(97): Show |
C | 3 | a0001c0001t0003g0042a0001c0003t0001g0004a0001c0003t0002g0004 | 4 | HG02622.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-544_637-441del | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | ||||||
chr22:35389320
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-544T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389320 | ||||||
chr22:35389320
|
TTCTTTCT others(68): Show |
T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.637-543_637-469del others(75): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389320 | ||||||
chr22:35389321
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0002g0053a0001c0001t0002g0059others(5): Show | 8 | HG02055.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-543T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389321 | ||||||
chr22:35389321
|
T | TTTCTTC | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0032 | 3 | HG02258.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-543_637-542ins others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389321 | ||||||
chr22:35389322
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.637-542C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389322 | ||||||
chr22:35389323
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 119 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.637-541T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389323 | ||||||
chr22:35389324
|
T | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0066others(4): Show | 7 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-540T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389324 | ||||||
chr22:35389325
|
T | C | 1 | a0001c0001t0001g0344 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637-539T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389325 | ||||||
chr22:35389326
|
CTTTCTTT others(70): Show |
C | 2 | a0001c0001t0001g0055a0001c0001t0001g0066 | 2 | HG02135.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.637-537_637-461del others(77): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389326 | ||||||
chr22:35389326
|
CTTTCTTT others(74): Show |
C | 1 | a0001c0001t0001g0067 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.637-537_637-457del others(81): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389326 | ||||||
chr22:35389326
|
CTTTCTTT others(82): Show |
C | 1 | a0001c0003t0001g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637-537_637-449del others(89): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389326 | ||||||
chr22:35389328
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0010g0182 | 3 | HG01243.hp2 HG01496.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.637-536T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389328 | ||||||
chr22:35389329
|
T | C | 1 | a0001c0001t0001g0344 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637-535T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389329 | ||||||
chr22:35389329
|
T | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-535T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389329 | ||||||
chr22:35389330
|
CT | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0099a0001c0001t0001g0166others(1): Show | 5 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-531delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389330 | |||||
chr22:35389330
|
CTTTCTTT others(66): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.637-533_637-461del others(73): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389330 | ||||||
chr22:35389331
|
T | C | 1 | a0002c0002t0001g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.637-533T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389331 | ||||||
chr22:35389331
|
TTTCTTTC others(57): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-532_637-469del others(64): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389331 | ||||||
chr22:35389332
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-532T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389332 | ||||||
chr22:35389332
|
TTCTTTCT others(91): Show |
T | 5 | a0001c0001t0002g0053a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-523_637-426del others(98): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389332 | |||||
chr22:35389333
|
T | C | 3 | a0001c0001t0001g0344a0001c0001t0010g0182a0005c0008t0001g0345 | 3 | HG01168.hp1 HG01496.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.637-531T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389333 | ||||||
chr22:35389335
|
T | C | 2 | a0001c0001t0001g0179a0002c0002t0001g0302 | 2 | HG00735.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.637-529T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389335 | ||||||
chr22:35389336
|
T | C | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-528T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389336 | ||||||
chr22:35389337
|
T | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0281a0001c0001t0001g0344others(1): Show | 4 | HG01168.hp1 HG01516.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-527T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389337 | ||||||
chr22:35389337
|
TCTTCTCC others(51): Show |
T | 1 | a0001c0001t0002g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637-523_637-466del others(58): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389337 | |||||
chr22:35389339
|
T | C | 4 | a0001c0001t0001g0179a0001c0001t0001g0270a0001c0001t0010g0182others(1): Show | 4 | HG00735.hp2 HG01496.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-525T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389339 | ||||||
chr22:35389339
|
T | TTTCTTTC others(88): Show |
1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.637-524_637-523ins others(95): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | |||||
chr22:35389339
|
T | TTTCTTTC others(94): Show |
1 | a0001c0001t0002g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(101): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | |||||
chr22:35389339
|
T | TTTCTTTC others(86): Show |
1 | a0001c0001t0002g0033 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(93): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | |||||
chr22:35389339
|
TTC | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0099a0001c0001t0001g0166others(2): Show | 6 | HG01109.hp1 HG01168.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-522_637-521del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | |||||
chr22:35389340
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.637-524T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | ||||||
chr22:35389340
|
T | TTCTTCTT others(14): Show |
1 | a0001c0001t0001g0289 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(21): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | ||||||
chr22:35389340
|
T | TTCTTTCT others(96): Show |
1 | a0001c0001t0002g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(103): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | ||||||
chr22:35389340
|
T | TTCTTTCT others(88): Show |
1 | a0001c0001t0002g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.637-524_637-523ins others(95): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | ||||||
chr22:35389340
|
TC | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0270a0002c0002t0001g0302 | 3 | HG00735.hp2 NA19078.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.637-523delC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | ||||||
chr22:35389340
|
TCTCCTTC others(83): Show |
T | 2 | a0001c0001t0001g0027a0001c0001t0012g0024 | 2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.637-523_637-434del others(90): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | ||||||
chr22:35389341
|
C | CTCCT | 17 | a0001c0001t0001g0019a0001c0001t0001g0190a0001c0001t0001g0192others(14): Show | 18 | HG00408.hp2 HG00621.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.637-469_637-466dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | CTCCTTCC others(1): Show |
8 | a0001c0001t0001g0018a0001c0001t0001g0247a0001c0001t0001g0248others(5): Show | 9 | HG00673.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.637-473_637-466dup others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | CTCCTTCC others(5): Show |
2 | a0001c0001t0001g0272a0001c0001t0001g0330 | 2 | HG01433.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.637-477_637-466dup others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | CTCCTTCC others(9): Show |
3 | a0001c0001t0001g0244a0001c0001t0001g0313a0001c0001t0001g0327 | 3 | HG03209.hp2 NA18944.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.637-481_637-466dup others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | CTCCTTCC others(13): Show |
1 | a0002c0002t0001g0301 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.637-485_637-466dup others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | CTCCTTCC others(37): Show |
1 | a0001c0001t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.637-509_637-466dup others(44): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | CTCCTTCC others(73): Show |
1 | a0001c0001t0001g0178 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(80): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0002g0029a0002c0002t0001g0264 | 3 | HG00642.hp2 HG02258.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.637-523C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389341 | ||||||
chr22:35389341
|
CTCCT | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0001g0085others(15): Show | 20 | HG00323.hp1 HG00544.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.637-469_637-466del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
CTCCTTCC others(1): Show |
C | 12 | a0001c0001t0001g0006a0001c0001t0001g0122a0001c0001t0001g0136others(9): Show | 14 | HG01978.hp1 HG02027.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-473_637-466del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
CTCCTTCC others(5): Show |
C | 19 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0092others(16): Show | 20 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.637-477_637-466del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
CTCCTTCC others(9): Show |
C | 7 | a0001c0001t0001g0091a0001c0001t0001g0111a0001c0001t0001g0138others(4): Show | 7 | HG00423.hp1 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-481_637-466del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389341
|
CTCCTTCC others(17): Show |
C | 1 | a0002c0002t0001g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.637-489_637-466del others(24): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | |||||
chr22:35389342
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.637-522T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389342 | ||||||
chr22:35389343
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0099a0001c0001t0001g0166others(1): Show | 5 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-521C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389343 | ||||||
chr22:35389343
|
CCTTCCTT others(3): Show |
C | 1 | a0001c0001t0001g0278 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.637-520_637-511del others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389343 | ||||||
chr22:35389344
|
C | T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-520C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389344 | ||||||
chr22:35389345
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0010g0182a0001c0011t0001g0041 | 3 | HG00423.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-519T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389345 | ||||||
chr22:35389347
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0099others(1): Show | 6 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-517C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389347 | ||||||
chr22:35389348
|
C | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-516C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389348 | ||||||
chr22:35389348
|
C | T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-516C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389348 | ||||||
chr22:35389349
|
T | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-515T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389349 | ||||||
chr22:35389351
|
C | CCTTCCTT others(8): Show |
1 | a0001c0001t0001g0207 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.637-511_637-497dup others(15): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389351 | |||||
chr22:35389351
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0218 | 3 | NA18940.hp2 NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.637-513C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389351 | ||||||
chr22:35389351
|
CCT | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0099a0001c0001t0001g0166others(1): Show | 5 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-512_637-511del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389351 | ||||||
chr22:35389352
|
C | T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-512C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389352 | ||||||
chr22:35389353
|
T | C | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-511T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389353 | ||||||
chr22:35389355
|
C | T | 1 | a0001c0001t0001g0014 | 2 | NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.637-509C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389355 | ||||||
chr22:35389356
|
C | T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-508C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389356 | ||||||
chr22:35389357
|
T | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-507T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389357 | ||||||
chr22:35389360
|
C | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-504C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389360 | ||||||
chr22:35389361
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-503T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389361 | ||||||
chr22:35389361
|
TTCCTTCC others(27): Show |
T | 1 | a0001c0011t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-502_637-469del others(34): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389361 | ||||||
chr22:35389367
|
CCTTCCTT others(37): Show |
C | 1 | a0001c0004t0004g0195 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637-493_637-450del others(44): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389367 | |||||
chr22:35389369
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-495T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389369 | ||||||
chr22:35389372
|
C | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-492C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389372 | ||||||
chr22:35389373
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-491T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389373 | ||||||
chr22:35389375
|
C | T | 3 | a0002c0002t0001g0304a0002c0002t0001g0306a0002c0002t0001g0307 | 3 | NA18957.hp2 NA18989.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.637-489C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389375 | ||||||
chr22:35389379
|
C | T | 1 | a0002c0002t0001g0306 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.637-485C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389379 | ||||||
chr22:35389379
|
CCTTCCTT others(13): Show |
C | 9 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0124others(6): Show | 9 | HG00597.hp2 HG01256.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-481_637-462del others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389379 | |||||
chr22:35389379
|
CCTTCCTT others(29): Show |
C | 1 | a0001c0001t0001g0073 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.637-481_637-446del others(36): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389379 | |||||
chr22:35389380
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-484C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389380 | ||||||
chr22:35389381
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-483T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389381 | ||||||
chr22:35389382
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-482T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389382 | ||||||
chr22:35389383
|
C | CCTTT | 4 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0176others(1): Show | 4 | HG01070.hp1 NA18952.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-478_637-477ins others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | |||||
chr22:35389383
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0001g0137a0001c0001t0001g0155others(1): Show | 4 | NA18971.hp2 NA18990.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-481C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389383 | ||||||
chr22:35389383
|
CCTTCCTT others(9): Show |
C | 8 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0090others(5): Show | 11 | HG01069.hp2 HG01255.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-477_637-462del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | |||||
chr22:35389383
|
CCTTCCTT others(13): Show |
C | 4 | a0001c0001t0001g0089a0001c0001t0001g0121a0001c0001t0001g0164others(1): Show | 4 | HG00438.hp2 HG02602.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-477_637-458del others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | |||||
chr22:35389383
|
CCTTCCTT others(21): Show |
C | 1 | a0001c0004t0004g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.637-477_637-450del others(28): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | |||||
chr22:35389384
|
C | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-480C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389384 | ||||||
chr22:35389384
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-480C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389384 | ||||||
chr22:35389385
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-479T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389385 | ||||||
chr22:35389387
|
C | CCCTCCCT others(87): Show |
1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(94): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | |||||
chr22:35389387
|
C | CCCTCCCT others(91): Show |
1 | a0001c0001t0001g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(98): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | |||||
chr22:35389387
|
C | CCCTCCCT others(85): Show |
1 | a0001c0001t0001g0102 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(92): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | |||||
chr22:35389387
|
C | T | 18 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0098others(15): Show | 19 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.637-477C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389387 | ||||||
chr22:35389387
|
CCTTCCTT others(5): Show |
C | 4 | a0001c0001t0001g0110a0001c0001t0001g0137a0001c0001t0001g0228others(1): Show | 4 | HG00609.hp1 HG02004.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-473_637-462del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | |||||
chr22:35389387
|
CCTTCCTT others(9): Show |
C | 1 | a0001c0001t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-473_637-458del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | |||||
chr22:35389389
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.637-475T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389389 | ||||||
chr22:35389390
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-474T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389390 | ||||||
chr22:35389391
|
C | CCTTCCTT others(21): Show |
1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(28): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389391
|
C | CCTTTCTT others(17): Show |
1 | a0001c0001t0004g0075 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.637-470_637-469ins others(24): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389391
|
C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.637-470_637-469ins others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389391
|
C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0154 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.637-470_637-469ins others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389391
|
C | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0080others(37): Show | 42 | HG01070.hp1 HG01167.hp2 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.637-473C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389391 | ||||||
chr22:35389391
|
CCTTCCTT others(1): Show |
C | 13 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0098others(10): Show | 14 | HG00558.hp2 HG00733.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-469_637-462del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389391
|
CCTTCCTT others(5): Show |
C | 3 | a0001c0001t0001g0254a0001c0001t0001g0310a0001c0001t0001g0341 | 3 | HG02132.hp1 HG03130.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.637-469_637-458del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389391
|
CCTTCCTT others(9): Show |
C | 1 | a0001c0001t0001g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.637-469_637-454del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | |||||
chr22:35389394
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-470T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389394 | ||||||
chr22:35389394
|
TCCTTTCT others(29): Show |
T | 1 | a0001c0001t0001g0346 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.637-469_637-434del others(36): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389394 | ||||||
chr22:35389395
|
C | CCTTCCTT others(40): Show |
1 | a0001c0001t0001g0159 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(47): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(69): Show |
1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(76): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(85): Show |
1 | a0001c0001t0001g0113 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(92): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(73): Show |
1 | a0001c0001t0005g0148 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(80): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(97): Show |
1 | a0001c0001t0001g0152 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(104): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(60): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(61): Show |
1 | a0001c0001t0001g0157 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(68): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(57): Show |
1 | a0001c0001t0005g0093 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(64): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0096 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(60): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(89): Show |
1 | a0001c0001t0001g0101 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(96): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(38): Show |
1 | a0001c0001t0001g0095 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(45): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(33): Show |
1 | a0001c0001t0001g0337 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(40): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(49): Show |
1 | a0001c0001t0001g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(56): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(17): Show |
1 | a0001c0001t0001g0311 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(24): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(25): Show |
1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(32): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(33): Show |
1 | a0001c0001t0001g0165 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(40): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(45): Show |
1 | a0001c0001t0001g0127 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(52): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(60): Show |
1 | a0001c0001t0001g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(67): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(9): Show |
1 | a0001c0001t0001g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(13): Show |
1 | a0001c0001t0001g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(5): Show |
1 | a0001c0001t0001g0249 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(60): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(1): Show |
5 | a0001c0001t0001g0129a0001c0001t0001g0197a0001c0001t0001g0221others(2): Show | 5 | HG00140.hp2 HG04184.hp2 NA19087.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-466_637-465ins others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(21): Show |
1 | a0001c0001t0006g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(28): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTCCTT others(5): Show |
2 | a0001c0001t0001g0277a0006c0010t0001g0294 | 2 | HG01081.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.637-466_637-465ins others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTT | 6 | a0001c0001t0001g0209a0001c0001t0001g0224a0001c0001t0001g0332others(3): Show | 6 | HG03831.hp2 HG04228.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-438_637-435dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTTCTT others(1): Show |
4 | a0001c0001t0001g0080a0001c0001t0001g0103a0001c0001t0004g0077others(1): Show | 4 | HG01358.hp2 HG02258.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-442_637-435dup others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | CCTTTCTT others(5): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0117a0001c0001t0001g0179 | 3 | HG00735.hp1 HG00735.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.637-446_637-435dup others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
C | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-469C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389395 | ||||||
chr22:35389395
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0017others(34): Show | 44 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.637-469C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389395 | ||||||
chr22:35389395
|
CCTTT | C | 12 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0193others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-438_637-435del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389395
|
CCTTTCTT others(1): Show |
C | 6 | a0001c0001t0001g0223a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-442_637-435del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | |||||
chr22:35389396
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-468C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389396 | ||||||
chr22:35389398
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0010g0182others(1): Show | 4 | HG01243.hp2 HG01496.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-466T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389398 | ||||||
chr22:35389399
|
T | C | 49 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(46): Show | 52 | HG00408.hp2 HG00733.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.637-465T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389399 | ||||||
chr22:35389401
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0010g0182 | 2 | HG01496.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.637-463T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389401 | ||||||
chr22:35389402
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0010g0182a0001c0006t0002g0350others(1): Show | 4 | HG01243.hp2 HG01496.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-462T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389402 | ||||||
chr22:35389403
|
T | C | 47 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0086others(44): Show | 47 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.637-461T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389403 | ||||||
chr22:35389405
|
T | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-459T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389405 | ||||||
chr22:35389406
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0010g0182a0001c0011t0001g0041 | 3 | HG01243.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-458T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389406 | ||||||
chr22:35389407
|
T | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(29): Show | 37 | HG00597.hp2 HG00733.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.637-457T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389407 | ||||||
chr22:35389407
|
T | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-457T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389407 | ||||||
chr22:35389410
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0010g0182a0001c0011t0001g0041 | 3 | HG01243.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-454T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389410 | ||||||
chr22:35389410
|
TTCTTTCT others(13): Show |
T | 1 | a0001c0006t0002g0350 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.637-434_637-415del others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389410 | |||||
chr22:35389411
|
T | C | 13 | a0001c0001t0001g0089a0001c0001t0001g0121a0001c0001t0001g0156others(10): Show | 13 | HG01192.hp2 HG02258.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.637-453T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389411 | ||||||
chr22:35389414
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0010g0182a0001c0011t0001g0041 | 3 | HG01243.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-450T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389414 | ||||||
chr22:35389414
|
TTCTTTCT others(9): Show |
T | 2 | a0001c0001t0001g0074a0001c0001t0001g0126 | 2 | HG02922.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.637-434_637-419del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389414 | |||||
chr22:35389415
|
T | C | 4 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0032others(1): Show | 4 | HG01192.hp2 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-449T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389415 | ||||||
chr22:35389416
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.637-448C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389416 | ||||||
chr22:35389418
|
T | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-446T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389418 | ||||||
chr22:35389418
|
TTCTTTCT others(5): Show |
T | 5 | a0001c0001t0001g0013a0001c0001t0001g0087a0001c0001t0001g0150others(2): Show | 6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-434_637-423del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389418 | |||||
chr22:35389419
|
T | C | 5 | a0001c0001t0001g0064a0001c0001t0002g0029a0001c0001t0002g0030others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-445T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389419 | ||||||
chr22:35389420
|
CTTTCTTT others(22): Show |
C | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.637-434_637-406del others(29): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389420 | |||||
chr22:35389421
|
T | TTTTTTCC others(58): Show |
1 | a0001c0001t0001g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.637-441_637-440ins others(65): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389421 | |||||
chr22:35389422
|
T | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-442T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389422 | ||||||
chr22:35389422
|
TTCTTTCT others(1): Show |
T | 5 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp1 HG03017.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-434_637-427del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389422 | |||||
chr22:35389423
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0002g0030 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-441T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389423 | ||||||
chr22:35389426
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0285 | 3 | HG01106.hp1 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.637-438T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389426 | ||||||
chr22:35389426
|
T | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-438T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389426 | ||||||
chr22:35389426
|
TTCTA | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0118a0001c0001t0001g0173others(1): Show | 5 | HG01175.hp1 HG01257.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-434_637-431del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389426 | |||||
chr22:35389428
|
CTATCTTT others(14): Show |
C | 1 | a0001c0001t0001g0342 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.637-434_637-414del others(21): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389428 | |||||
chr22:35389430
|
A | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-434A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389430 | ||||||
chr22:35389430
|
A | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(162): Show | 174 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.637-434A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389430 | ||||||
chr22:35389434
|
T | A | 1 | a0001c0001t0001g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.637-430T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389434 | ||||||
chr22:35389434
|
T | C | 2 | a0001c0001t0010g0182a0001c0011t0001g0041 | 2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-430T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389434 | ||||||
chr22:35389438
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-426T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389438 | ||||||
chr22:35389440
|
C | CTTTCT | 3 | a0001c0001t0001g0015a0001c0001t0001g0274a0001c0001t0001g0285 | 4 | HG01106.hp1 HG01192.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-421_637-417dup others(5): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389440 | |||||
chr22:35389441
|
T | G | 1 | a0001c0001t0002g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-423T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389441 | ||||||
chr22:35389442
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-422T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389442 | ||||||
chr22:35389445
|
T | G | 1 | a0001c0001t0002g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-419T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389445 | ||||||
chr22:35389445
|
TTTCTTTT others(5): Show |
T | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-416_637-405del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389445 | |||||
chr22:35389446
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-418T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389446 | ||||||
chr22:35389448
|
CT | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(53): Show | 59 | HG00408.hp1 HG00597.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.637-412delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389448 | |||||
chr22:35389450
|
T | G | 1 | a0001c0001t0002g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-414T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389450 | ||||||
chr22:35389451
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-413T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389451 | ||||||
chr22:35389452
|
T | C | 9 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0126others(6): Show | 9 | HG00597.hp2 NA18948.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-412T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389452 | ||||||
chr22:35389453
|
C | T | 6 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0158others(3): Show | 6 | NA18968.hp1 NA18971.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-411C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389453 | ||||||
chr22:35389455
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-409T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389455 | ||||||
chr22:35389459
|
T | C | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-405T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389459 | ||||||
chr22:35389464
|
G | T | 3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0032 | 3 | HG02258.hp2 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-400G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389464 | ||||||
chr22:35389466
|
A | T | 3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0032 | 3 | HG02258.hp2 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-398A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389466 | ||||||
chr22:35389474
|
G | A | 8 | a0002c0002t0001g0021a0002c0002t0001g0300a0002c0002t0001g0304others(5): Show | 9 | HG00544.hp2 HG00673.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.637-390G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389474 | ||||||
chr22:35389486
|
G | A | 60 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(57): Show | 64 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.637-378G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389486 | ||||||
chr22:35389517
|
A | T | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-347A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389517 | ||||||
chr22:35389675
|
C | CT | 179 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.637-189_637-188ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389675 | ||||||
chr22:35389681
|
T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-183T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389681 | ||||||
chr22:35389706
|
G | A | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-158G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389706 | ||||||
chr22:35389710
|
G | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(56): Show | 63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.637-154G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389710 | ||||||
chr22:35390010
|
GGACTTGG others(6): Show |
G | 8 | a0002c0002t0001g0021a0002c0002t0001g0300a0002c0002t0001g0304others(5): Show | 9 | HG00544.hp2 HG00673.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+52_736+64delTG others(11): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35390010 | |||||
chr22:35390022
|
C | G | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.736+59C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390022 | ||||||
chr22:35390117
|
G | T | 2 | a0001c0004t0004g0195a0001c0004t0004g0196 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.736+154G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390117 | ||||||
chr22:35390123
|
G | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0158others(2): Show | 5 | NA18968.hp1 NA18971.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+160G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390123 | ||||||
chr22:35390189
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(186): Show | 201 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.736+226A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390189 | ||||||
chr22:35390233
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+270T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390233 | ||||||
chr22:35390272
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.736+309G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390272 | ||||||
chr22:35390618
|
T | G | 11 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0131others(8): Show | 11 | HG00423.hp1 HG00609.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.736+655T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390618 | ||||||
chr22:35390620
|
T | C | 1 | a0002c0002t0001g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.736+657T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390620 | ||||||
chr22:35390666
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.736+703A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390666 | ||||||
chr22:35390713
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+750A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390713 | ||||||
chr22:35390720
|
A | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+757A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390720 | ||||||
chr22:35390729
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.736+766T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390729 | ||||||
chr22:35390748
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+785T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390748 | ||||||
chr22:35390880
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+917A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390880 | ||||||
chr22:35390970
|
G | A | 53 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(50): Show | 56 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.736+1007G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390970 | ||||||
chr22:35390994
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+1031T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390994 | ||||||
chr22:35391012
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+1049G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391012 | ||||||
chr22:35391072
|
T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+1109T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391072 | ||||||
chr22:35391106
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.736+1143C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391106 | ||||||
chr22:35391171
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.736+1208C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391171 | ||||||
chr22:35391173
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.736+1210C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391173 | ||||||
chr22:35391174
|
C | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1211C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391174 | ||||||
chr22:35391218
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.736+1255G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391218 | ||||||
chr22:35391242
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1279C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391242 | ||||||
chr22:35391257
|
CA | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1297delA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391257 | |||||
chr22:35391283
|
ATTTTTTT others(11): Show |
A | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1324_736+1341d others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391283 | |||||
chr22:35391292
|
G | GT | 20 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0001g0201others(17): Show | 21 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.736+1341dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391292 | |||||
chr22:35391292
|
GT | G | 7 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(4): Show | 7 | HG01192.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.736+1341delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391292 | |||||
chr22:35391327
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.736+1364A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391327 | ||||||
chr22:35391328
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.736+1365C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391328 | ||||||
chr22:35391337
|
G | A | 8 | a0001c0001t0001g0153a0002c0002t0001g0021a0002c0002t0001g0304others(5): Show | 9 | HG00544.hp2 HG00673.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+1374G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391337 | ||||||
chr22:35391356
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1393C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391356 | ||||||
chr22:35391373
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.736+1410C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391373 | ||||||
chr22:35391413
|
G | A | 2 | a0001c0001t0010g0182a0003c0009t0001g0023 | 2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1450G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391413 | ||||||
chr22:35391437
|
G | A | 2 | a0001c0001t0010g0182a0003c0009t0001g0023 | 2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1474G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391437 | ||||||
chr22:35391444
|
T | C | 2 | a0001c0001t0010g0182a0003c0009t0001g0023 | 2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1481T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391444 | ||||||
chr22:35391508
|
C | T | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.736+1545C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391508 | ||||||
chr22:35391522
|
T | C | 2 | a0001c0001t0010g0182a0003c0009t0001g0023 | 2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1559T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391522 | ||||||
chr22:35391557
|
A | C | 2 | a0001c0001t0010g0182a0003c0009t0001g0023 | 2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1594A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391557 | ||||||
chr22:35391579
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.736+1616G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391579 | ||||||
chr22:35391582
|
C | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+1619C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391582 | ||||||
chr22:35391585
|
C | CAT | 74 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 79 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.736+1622_736+1623i others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391585 | ||||||
chr22:35391585
|
C | CATT | 33 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0079others(30): Show | 34 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.736+1622_736+1623i others(5): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391585 | ||||||
chr22:35391585
|
C | CATTT | 9 | a0001c0001t0001g0013a0001c0001t0001g0082a0001c0001t0001g0120others(6): Show | 10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.736+1622_736+1623i others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391585 | ||||||
chr22:35391586
|
C | CT | 58 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0025others(55): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.736+1648dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | |||||
chr22:35391586
|
C | CTT | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0026others(31): Show | 37 | HG00408.hp1 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.736+1647_736+1648d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | |||||
chr22:35391586
|
C | CTTT | 24 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(21): Show | 24 | HG01175.hp2 HG01243.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.736+1646_736+1648d others(5): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | |||||
chr22:35391586
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1623C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391586 | ||||||
chr22:35391586
|
CT | C | 11 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0226others(8): Show | 12 | HG00544.hp2 HG00673.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.736+1648delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | |||||
chr22:35391625
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1662G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391625 | ||||||
chr22:35391755
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.737-1713A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391755 | ||||||
chr22:35391757
|
A | AT | 42 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0025others(39): Show | 45 | HG00408.hp1 HG00423.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.737-1697dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391757 | |||||
chr22:35391757
|
AT | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.737-1697delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391757 | |||||
chr22:35391758
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.737-1710T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391758 | ||||||
chr22:35391771
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-1697T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391771 | ||||||
chr22:35391773
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-1695G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391773 | ||||||
chr22:35391774
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-1694C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391774 | ||||||
chr22:35391966
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737-1502T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391966 | ||||||
chr22:35391990
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.737-1478T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391990 | ||||||
chr22:35392149
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-1319G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392149 | ||||||
chr22:35392221
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.737-1231dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392221 | |||||
chr22:35392221
|
C | CAA | 6 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0108others(3): Show | 6 | HG01069.hp2 HG01243.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.737-1232_737-1231d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392221 | |||||
chr22:35392256
|
A | AAGAATTT others(24): Show |
1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-1210_737-1180d others(33): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392256 | |||||
chr22:35392606
|
G | A | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.737-862G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392606 | ||||||
chr22:35392607
|
G | T | 1 | a0001c0001t0010g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.737-861G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392607 | ||||||
chr22:35392717
|
C | CT | 10 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0086others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-733dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392717 | |||||
chr22:35392717
|
CT | C | 9 | a0001c0001t0001g0043a0001c0001t0001g0081a0001c0001t0001g0126others(6): Show | 9 | HG01168.hp1 HG01517.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-733delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392717 | |||||
chr22:35392779
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.737-689G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392779 | ||||||
chr22:35392841
|
C | T | 6 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(3): Show | 6 | HG02027.hp1 HG02056.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-627C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392841 | ||||||
chr22:35392891
|
T | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-577T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392891 | ||||||
chr22:35392892
|
A | T | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-576A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392892 | ||||||
chr22:35392893
|
T | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-575T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392893 | ||||||
chr22:35392916
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 123 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.737-552C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392916 | ||||||
chr22:35392976
|
A | T | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-492A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392976 | ||||||
chr22:35392988
|
T | G | 3 | a0001c0001t0001g0310a0001c0001t0001g0318a0001c0001t0001g0331 | 3 | HG01175.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.737-480T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392988 | ||||||
chr22:35393011
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-457C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393011 | ||||||
chr22:35393053
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737-415G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393053 | ||||||
chr22:35393114
|
A | C | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-354A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393114 | ||||||
chr22:35393115
|
C | G | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-353C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393115 | ||||||
chr22:35393116
|
G | T | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-352G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393116 | ||||||
chr22:35393149
|
C | G | 1 | a0002c0002t0001g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.737-319C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393149 | ||||||
chr22:35393207
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.737-261C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393207 | ||||||
chr22:35393251
|
G | T | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-217G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393251 | ||||||
chr22:35393268
|
T | A | 3 | a0002c0002t0001g0300a0002c0002t0002g0298a0002c0002t0002g0299 | 3 | HG02809.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.737-200T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393268 | ||||||
chr22:35393270
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(181): Show | 195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.737-198A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393270 | ||||||
chr22:35393288
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.737-180C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393288 | ||||||
chr22:35393325
|
C | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-143C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393325 | ||||||
chr22:35393386
|
C | T | 3 | a0002c0002t0001g0300a0002c0002t0002g0298a0002c0002t0002g0299 | 3 | HG02809.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.737-82C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393386 | ||||||
chr22:35393399
|
T | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-69T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393399 | ||||||
chr22:35393400
|
T | C | 1 | a0001c0001t0009g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.737-68T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393400 | ||||||
chr22:35393405
|
A | G | 1 | a0003c0009t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.737-63A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393405 | ||||||
chr22:35393406
|
T | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-62T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393406 | ||||||
chr22:35393448
|
T | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-20T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393448 | ||||||
chr22:35393452
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.737-16C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393452 | ||||||
chr22:35393457
|
T | A | 1 | a0004c0007t0011g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-11T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393457 |