geneid | 48 |
---|---|
ensemblid | ENSG00000122729.19 |
hgncid | 117 |
symbol | ACO1 |
name | aconitase 1 |
refseq_nuc | NM_002197.3 |
refseq_prot | NP_002188.1 |
ensembl_nuc | ENST00000309951.8 |
ensembl_prot | ENSP00000309477.5 |
mane_status | MANE Select |
chr | chr9 |
start | 32384643 |
end | 32454769 |
strand | + |
ver | v1.2 |
region | chr9:32384643-32454769 |
region5000 | chr9:32379643-32459769 |
regionname0 | ACO1_chr9_32384643_32454769 |
regionname5000 | ACO1_chr9_32379643_32459769 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 889 | 346 | 75 | 63 | 145 | 16 | 45 | 112 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002 | 0/0 | 889 | 13 | 11 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0003 | 0/0 | 889 | 8 | 0 | 0 | 8 | 0 | 0 | 5 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0004 | 0/0 | 889 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0005 | 0/0 | 889 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0006 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0007 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0008 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0009 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0010 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0011 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0012 | 0/0 | 889 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0013 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0014 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0015 | 0/0 | 889 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2670 | 178 | 35 | 37 | 63 | 11 | 31 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0002 | 0/1 | 2670 | 144 | 18 | 24 | 82 | 5 | 14 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0003 | 0/0 | 2670 | 8 | 0 | 0 | 8 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0004 | 0/0 | 2670 | 8 | 6 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0005 | 0/0 | 2670 | 6 | 6 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0006 | 0/0 | 2670 | 6 | 6 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0007 | 0/0 | 2670 | 5 | 5 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0008 | 0/0 | 2670 | 2 | 1 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0009 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0010 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0011 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0012 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0013 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0014 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0015 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0016 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0017 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0018 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0019 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0020 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0021 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0022 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0023 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0024 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0025 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0026 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0027 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0028 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
c0029 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4775 | 46 | 7 | 1 | 30 | 0 | 8 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0002 | 0/0 | 4774 | 32 | 2 | 6 | 23 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0003 | 0/0 | 4775 | 30 | 12 | 9 | 8 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0004 | 0/1 | 4776 | 24 | 0 | 7 | 12 | 4 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0005 | 0/0 | 4776 | 14 | 1 | 0 | 6 | 0 | 7 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0006 | 0/0 | 4775 | 14 | 1 | 3 | 3 | 1 | 6 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0007 | 0/0 | 4780 | 12 | 1 | 4 | 0 | 3 | 4 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0008 | 0/0 | 4780 | 11 | 10 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0009 | 0/0 | 4776 | 11 | 0 | 0 | 11 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0010 | 0/0 | 4775 | 8 | 0 | 1 | 5 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0011 | 0/0 | 4776 | 6 | 0 | 3 | 0 | 2 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0012 | 0/0 | 4777 | 6 | 0 | 2 | 3 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0013 | 0/0 | 4778 | 6 | 6 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0014 | 0/0 | 4774 | 6 | 3 | 1 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0015 | 0/0 | 4776 | 6 | 1 | 1 | 1 | 0 | 3 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0016 | 0/0 | 4775 | 5 | 0 | 0 | 4 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0017 | 0/0 | 4775 | 5 | 0 | 0 | 5 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0018 | 0/0 | 4779 | 5 | 5 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0019 | 0/0 | 4774 | 4 | 2 | 0 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0020 | 0/0 | 4775 | 4 | 0 | 3 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0021 | 0/0 | 4775 | 4 | 0 | 0 | 4 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0022 | 0/0 | 4775 | 4 | 0 | 0 | 4 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0023 | 0/0 | 4775 | 4 | 2 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0024 | 0/0 | 4776 | 3 | 3 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0025 | 0/0 | 4777 | 3 | 0 | 0 | 3 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0026 | 0/0 | 4775 | 3 | 0 | 2 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0027 | 0/0 | 4778 | 3 | 2 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0028 | 0/0 | 4827 | 3 | 3 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0029 | 0/0 | 4780 | 3 | 0 | 1 | 0 | 2 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0030 | 1/0 | 4774 | 3 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0031 | 0/0 | 4776 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0032 | 0/0 | 4827 | 2 | 1 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0033 | 0/0 | 4781 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0034 | 0/0 | 4780 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0035 | 0/0 | 4774 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0036 | 0/0 | 4774 | 2 | 1 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0037 | 0/0 | 4776 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0038 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0039 | 0/0 | 4778 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0040 | 0/0 | 4776 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0041 | 0/0 | 4776 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0042 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0043 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0044 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0045 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0046 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0047 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0048 | 0/0 | 4777 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0049 | 0/0 | 4776 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0050 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0051 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0052 | 0/0 | 4776 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0053 | 0/0 | 4775 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0054 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0055 | 0/0 | 4776 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0056 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0057 | 0/0 | 4777 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0058 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0059 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0060 | 0/0 | 4777 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0061 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0062 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0063 | 0/0 | 4777 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0064 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0065 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0066 | 0/0 | 4779 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0067 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0068 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0069 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0070 | 0/0 | 4776 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0071 | 0/0 | 4777 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0072 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0073 | 0/0 | 4827 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0074 | 0/0 | 4776 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0075 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0076 | 0/0 | 4780 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0077 | 0/0 | 4781 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0078 | 0/0 | 4780 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0079 | 0/0 | 4779 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0080 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0081 | 0/0 | 4778 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0082 | 0/0 | 4779 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0083 | 0/0 | 4778 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0084 | 0/0 | 4777 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0085 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0086 | 0/0 | 4777 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0087 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0088 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0089 | 0/0 | 4775 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0090 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0091 | 0/0 | 4775 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0092 | 0/0 | 4776 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0093 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0094 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0095 | 0/0 | 4777 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0096 | 0/0 | 4776 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0097 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0098 | 0/0 | 4777 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0099 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0100 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0101 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0102 | 0/0 | 4775 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0103 | 0/0 | 4774 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0104 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0105 | 0/0 | 4777 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0106 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0107 | 0/0 | 4775 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0108 | 0/0 | 4778 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0109 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0110 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0111 | 0/0 | 4778 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0112 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
t0113 | 0/0 | 4754 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0004 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2670 | 178 | 35 | 37 | 63 | 11 | 31 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002 | 0/1 | 2670 | 144 | 18 | 24 | 82 | 5 | 14 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0005 | 0/0 | 2670 | 6 | 6 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0006 | 0/0 | 2670 | 6 | 6 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0008 | 0/0 | 2670 | 2 | 1 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0010 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0011 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0018 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0019 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0022 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0023 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0025 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0026 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0004 | 0/0 | 2670 | 8 | 6 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0007 | 0/0 | 2670 | 5 | 5 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0003c0003 | 0/0 | 2670 | 8 | 0 | 0 | 8 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0004c0009 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0004c0027 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0005c0012 | 0/0 | 2670 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0006c0014 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0007c0016 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0008c0029 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0009c0024 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0010c0021 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0011c0020 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0012c0028 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0013c0017 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0014c0015 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0015c0013 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7444 | 34 | 5 | 1 | 22 | 0 | 6 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0002 | 0/0 | 7443 | 3 | 0 | 1 | 1 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0003 | 0/0 | 7444 | 25 | 11 | 9 | 4 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0004 | 0/0 | 7445 | 7 | 0 | 3 | 1 | 3 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0005 | 0/0 | 7445 | 12 | 1 | 0 | 5 | 0 | 6 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0006 | 0/0 | 7444 | 13 | 1 | 3 | 3 | 1 | 5 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0007 | 0/0 | 7449 | 8 | 1 | 2 | 0 | 2 | 3 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0010 | 0/0 | 7444 | 2 | 0 | 0 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0011 | 0/0 | 7445 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0014 | 0/0 | 7443 | 5 | 2 | 1 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0015 | 0/0 | 7445 | 5 | 1 | 1 | 1 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0016 | 0/0 | 7444 | 4 | 0 | 0 | 3 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0018 | 0/0 | 7448 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0019 | 0/0 | 7443 | 4 | 2 | 0 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0020 | 0/0 | 7444 | 4 | 0 | 3 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0021 | 0/0 | 7444 | 3 | 0 | 0 | 3 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0022 | 0/0 | 7444 | 3 | 0 | 0 | 3 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0024 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0025 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0029 | 0/0 | 7449 | 3 | 0 | 1 | 0 | 2 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0030 | 1/0 | 7443 | 3 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0033 | 0/0 | 7450 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0036 | 0/0 | 7443 | 2 | 1 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0039 | 0/0 | 7447 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0040 | 0/0 | 7445 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0052 | 0/0 | 7445 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0053 | 0/0 | 7444 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0054 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0069 | 0/0 | 7424 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0074 | 0/0 | 7445 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0075 | 0/0 | 7442 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0076 | 0/0 | 7449 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0077 | 0/0 | 7450 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0078 | 0/0 | 7449 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0080 | 0/0 | 7430 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0084 | 0/0 | 7446 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0085 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0086 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0087 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0088 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0089 | 0/0 | 7444 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0090 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0091 | 0/0 | 7444 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0092 | 0/0 | 7445 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0096 | 0/0 | 7445 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0097 | 0/0 | 7442 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0099 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0100 | 0/0 | 7442 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0101 | 0/0 | 7443 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0102 | 0/0 | 7444 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0106 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0111 | 0/0 | 7447 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0001t0113 | 0/0 | 7423 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0001 | 0/0 | 7444 | 8 | 0 | 0 | 6 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0002 | 0/0 | 7443 | 28 | 2 | 5 | 21 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0003 | 0/0 | 7444 | 4 | 0 | 0 | 4 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0004 | 0/1 | 7445 | 16 | 0 | 4 | 10 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0005 | 0/0 | 7445 | 2 | 0 | 0 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0006 | 0/0 | 7444 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0007 | 0/0 | 7449 | 3 | 0 | 1 | 0 | 1 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0008 | 0/0 | 7449 | 9 | 8 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0009 | 0/0 | 7445 | 11 | 0 | 0 | 11 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0010 | 0/0 | 7444 | 6 | 0 | 1 | 4 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0011 | 0/0 | 7445 | 5 | 0 | 2 | 0 | 2 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0012 | 0/0 | 7446 | 4 | 0 | 2 | 1 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0013 | 0/0 | 7447 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0016 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0021 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0022 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0025 | 0/0 | 7446 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0026 | 0/0 | 7444 | 3 | 0 | 2 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0027 | 0/0 | 7447 | 3 | 2 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0034 | 0/0 | 7449 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0035 | 0/0 | 7443 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0038 | 0/0 | 7424 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0041 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0045 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0046 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0047 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0048 | 0/0 | 7446 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0049 | 0/0 | 7445 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0050 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0055 | 0/0 | 7445 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0056 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0057 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0058 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0059 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0060 | 0/0 | 7446 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0061 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0062 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0063 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0065 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0067 | 0/0 | 7443 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0068 | 0/0 | 7415 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0070 | 0/0 | 7445 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0071 | 0/0 | 7446 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0082 | 0/0 | 7448 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0083 | 0/0 | 7447 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0093 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0094 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0095 | 0/0 | 7446 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0098 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0103 | 0/0 | 7443 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0107 | 0/0 | 7444 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0002t0108 | 0/0 | 7447 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0005t0013 | 0/0 | 7447 | 5 | 5 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0005t0081 | 0/0 | 7447 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0006t0003 | 0/0 | 7444 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0006t0018 | 0/0 | 7448 | 4 | 4 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0006t0105 | 0/0 | 7446 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0008t0032 | 0/0 | 7496 | 2 | 1 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0010t0028 | 0/0 | 7496 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0010t0072 | 0/0 | 7496 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0011t0109 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0011t0110 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0018t0034 | 0/0 | 7449 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0019t0112 | 0/0 | 7424 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0022t0073 | 0/0 | 7496 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0023t0066 | 0/0 | 7448 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0025t0028 | 0/0 | 7496 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0001c0026t0028 | 0/0 | 7496 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0004t0001 | 0/0 | 7444 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0004t0014 | 0/0 | 7443 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0004t0023 | 0/0 | 7444 | 4 | 2 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0004t0064 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0007t0031 | 0/0 | 7445 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0007t0042 | 0/0 | 7444 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0007t0043 | 0/0 | 7444 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0002c0007t0044 | 0/0 | 7424 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0003c0003t0004 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0003c0003t0017 | 0/0 | 7444 | 5 | 0 | 0 | 5 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0003c0003t0037 | 0/0 | 7445 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0004c0009t0024 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0004c0009t0051 | 0/0 | 7444 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0004c0027t0024 | 0/0 | 7445 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0005c0012t0008 | 0/0 | 7449 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0006c0014t0012 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0007c0016t0012 | 0/0 | 7446 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0008c0029t0002 | 0/0 | 7443 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0009c0024t0041 | 0/0 | 7445 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0010c0021t0079 | 0/0 | 7448 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0011c0020t0001 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0012c0028t0007 | 0/0 | 7449 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0013c0017t0104 | 0/0 | 7443 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0014c0015t0001 | 0/0 | 7444 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
a0015c0013t0015 | 0/0 | 7445 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | copy fasta | chr9 | 32379643 | 32459769 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0006g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0007g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0011g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0014g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0014g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0015g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0015g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0015g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0015g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0015g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0016g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0016g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0016g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0016g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0019g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0019g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0020g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0020g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0021g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0021g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0021g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0022g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0022g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0024g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0025g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0029g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0029g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0029g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0030g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0030g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0030g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0033g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0033g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0036g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0036g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0039g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0039g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0040g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0040g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0052g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0053g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0054g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0069g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0074g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0075g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0076g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0077g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0078g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0080g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0084g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0085g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0086g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0087g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0088g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0089g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0090g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0091g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0092g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0096g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0097g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0099g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0100g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0101g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0102g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0106g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0111g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0001t0113g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0006g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0007g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0009g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0010g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0010g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0010g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0010g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0011g0004 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0011g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0012g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0012g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0012g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0012g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0016g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0021g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0022g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0025g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0026g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0026g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0026g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0027g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0027g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0027g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0034g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0035g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0035g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0038g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0038g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0041g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0045g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0046g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0047g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0048g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0049g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0050g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0055g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0056g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0057g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0058g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0059g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0060g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0061g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0062g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0063g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0065g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0067g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0068g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0070g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0071g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0082g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0083g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0093g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0094g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0095g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0098g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0103g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0107g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0002t0108g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0005t0013g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0005t0013g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0005t0013g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0005t0013g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0005t0081g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0006t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0006t0018g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0006t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0006t0018g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0006t0105g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0008t0032g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0008t0032g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0010t0028g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0010t0072g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0011t0109g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0011t0110g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0018t0034g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0019t0112g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0022t0073g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0023t0066g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0025t0028g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0001c0026t0028g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0004t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0004t0023g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0004t0023g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0004t0064g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0007t0031g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0007t0031g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0007t0042g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0007t0043g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0002c0007t0044g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0017g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0017g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0017g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0017g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0017g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0003c0003t0037g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0004c0009t0024g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0004c0009t0051g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0004c0027t0024g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0005c0012t0008g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0006c0014t0012g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0007c0016t0012g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0008c0029t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0009c0024t0041g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0010c0021t0079g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0011c0020t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0012c0028t0007g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0013c0017t0104g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0014c0015t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
a0015c0013t0015g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0044 | EUR | GBR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00099 | hp2 | a0001 | c0002 | t0004 | g0242 | EUR | GBR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00140 | hp1 | a0001 | c0002 | t0055 | g0009 | EUR | GBR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0297 | EUR | GBR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00280 | hp1 | a0001 | c0001 | t0016 | g0118 | EUR | FIN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0149 | EUR | FIN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00323 | hp1 | a0001 | c0001 | t0102 | g0295 | EUR | FIN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00323 | hp2 | a0001 | c0002 | t0011 | g0004 | EUR | FIN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00423 | hp1 | a0001 | c0002 | t0010 | g0020 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00544 | hp1 | a0001 | c0001 | t0025 | g0200 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00544 | hp2 | a0001 | c0002 | t0010 | g0020 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00558 | hp2 | a0011 | c0020 | t0001 | g0188 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00597 | hp1 | a0001 | c0002 | t0009 | g0010 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00621 | hp1 | a0001 | c0002 | t0065 | g0116 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00621 | hp2 | a0001 | c0001 | t0021 | g0023 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00639 | hp1 | a0001 | c0001 | t0029 | g0017 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00639 | hp2 | a0001 | c0002 | t0010 | g0243 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00673 | hp2 | a0003 | c0003 | t0017 | g0191 | EAS | CHS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0030 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00735 | hp2 | a0001 | c0002 | t0012 | g0290 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00738 | hp1 | a0001 | c0001 | t0014 | g0154 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0273 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG00741 | hp2 | a0001 | c0001 | t0033 | g0147 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0291 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01070 | hp1 | a0001 | c0001 | t0096 | g0011 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01070 | hp2 | a0002 | c0004 | t0023 | g0008 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01071 | hp1 | a0002 | c0004 | t0023 | g0008 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0292 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01074 | hp1 | a0001 | c0001 | t0091 | g0085 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01081 | hp2 | a0001 | c0002 | t0026 | g0245 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01099 | hp2 | a0001 | c0002 | t0004 | g0287 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01106 | hp1 | a0001 | c0002 | t0011 | g0004 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01106 | hp2 | a0001 | c0001 | t0076 | g0061 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01109 | hp2 | a0001 | c0002 | t0007 | g0269 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01167 | hp1 | a0001 | c0001 | t0011 | g0184 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0294 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01175 | hp1 | a0001 | c0001 | t0053 | g0313 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01175 | hp2 | a0001 | c0002 | t0027 | g0309 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01192 | hp1 | a0001 | c0002 | t0012 | g0256 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01192 | hp2 | a0001 | c0022 | t0073 | g0169 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01243 | hp1 | a0001 | c0008 | t0032 | g0326 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01243 | hp2 | a0001 | c0002 | t0026 | g0274 | AMR | PUR | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01255 | hp1 | a0001 | c0002 | t0082 | g0320 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0227 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01256 | hp2 | a0001 | c0002 | t0035 | g0068 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01261 | hp1 | a0001 | c0001 | t0077 | g0017 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01346 | hp1 | a0001 | c0002 | t0004 | g0069 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01346 | hp2 | a0001 | c0002 | t0035 | g0233 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01358 | hp2 | a0012 | c0028 | t0007 | g0266 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01361 | hp1 | a0001 | c0002 | t0048 | g0299 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01361 | hp2 | a0001 | c0001 | t0015 | g0321 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01433 | hp2 | a0001 | c0001 | t0033 | g0145 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01496 | hp2 | a0001 | c0002 | t0008 | g0285 | AMR | CLM | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0153 | EUR | IBS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0311 | EUR | IBS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0030 | EUR | IBS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01517 | hp2 | a0001 | c0002 | t0011 | g0004 | EUR | IBS | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01891 | hp1 | a0002 | c0004 | t0023 | g0158 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01891 | hp2 | a0002 | c0007 | t0042 | g0096 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01934 | hp1 | a0001 | c0001 | t0020 | g0327 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01934 | hp2 | a0001 | c0001 | t0084 | g0267 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01978 | hp1 | a0001 | c0001 | t0092 | g0216 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01978 | hp2 | a0001 | c0001 | t0078 | g0146 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01981 | hp1 | a0001 | c0002 | t0049 | g0050 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01993 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0142 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02015 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02040 | hp1 | a0006 | c0014 | t0012 | g0251 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02040 | hp2 | a0001 | c0002 | t0058 | g0165 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02055 | hp1 | a0001 | c0002 | t0034 | g0222 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02055 | hp2 | a0001 | c0018 | t0034 | g0091 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02074 | hp1 | a0003 | c0003 | t0004 | g0209 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0247 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02129 | hp2 | a0001 | c0002 | t0009 | g0259 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02132 | hp1 | a0001 | c0002 | t0010 | g0332 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02132 | hp2 | a0003 | c0003 | t0017 | g0201 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02135 | hp2 | a0001 | c0002 | t0012 | g0280 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0047 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02145 | hp2 | a0001 | c0001 | t0054 | g0312 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02155 | hp1 | a0001 | c0001 | t0021 | g0190 | EAS | CDX | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | CDX | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02165 | hp1 | a0001 | c0001 | t0020 | g0001 | EAS | CDX | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02165 | hp2 | a0001 | c0002 | t0010 | g0150 | EAS | CDX | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02257 | hp1 | a0001 | c0002 | t0027 | g0303 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02258 | hp1 | a0001 | c0002 | t0008 | g0236 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02273 | hp1 | a0001 | c0001 | t0089 | g0005 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02273 | hp2 | a0001 | c0001 | t0020 | g0025 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02280 | hp2 | a0001 | c0006 | t0018 | g0032 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02293 | hp1 | a0001 | c0001 | t0020 | g0025 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02293 | hp2 | a0001 | c0002 | t0011 | g0060 | AMR | PEL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02451 | hp2 | a0001 | c0001 | t0113 | g0062 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02523 | hp1 | a0001 | c0002 | t0047 | g0262 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02523 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02572 | hp2 | a0001 | c0002 | t0038 | g0328 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0156 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02602 | hp2 | a0001 | c0002 | t0071 | g0275 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02622 | hp1 | a0013 | c0017 | t0104 | g0132 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02630 | hp1 | a0001 | c0002 | t0008 | g0225 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02630 | hp2 | a0001 | c0001 | t0090 | g0073 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02647 | hp2 | a0001 | c0002 | t0008 | g0302 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02698 | hp1 | a0001 | c0002 | t0103 | g0164 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02698 | hp2 | a0001 | c0001 | t0015 | g0035 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02717 | hp1 | a0002 | c0004 | t0023 | g0008 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02717 | hp2 | a0001 | c0010 | t0028 | g0066 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02723 | hp1 | a0002 | c0007 | t0031 | g0094 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02723 | hp2 | a0001 | c0001 | t0111 | g0139 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0034 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02738 | hp1 | a0001 | c0001 | t0097 | g0046 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02738 | hp2 | a0001 | c0002 | t0095 | g0298 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02809 | hp1 | a0001 | c0001 | t0036 | g0007 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02818 | hp1 | a0001 | c0005 | t0013 | g0304 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02818 | hp2 | a0001 | c0026 | t0028 | g0319 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02886 | hp1 | a0001 | c0002 | t0083 | g0300 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02886 | hp2 | a0001 | c0001 | t0080 | g0323 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02895 | hp1 | a0001 | c0002 | t0013 | g0064 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02895 | hp2 | a0005 | c0012 | t0008 | g0027 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02896 | hp1 | a0001 | c0001 | t0019 | g0007 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02896 | hp2 | a0001 | c0005 | t0013 | g0029 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02897 | hp1 | a0001 | c0005 | t0013 | g0029 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02897 | hp2 | a0005 | c0012 | t0008 | g0027 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02922 | hp1 | a0001 | c0005 | t0013 | g0317 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02922 | hp2 | a0002 | c0004 | t0001 | g0137 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02965 | hp1 | a0001 | c0023 | t0066 | g0220 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02965 | hp2 | a0001 | c0001 | t0030 | g0160 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02970 | hp1 | a0001 | c0005 | t0081 | g0314 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02970 | hp2 | a0002 | c0004 | t0001 | g0135 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02976 | hp1 | a0001 | c0019 | t0112 | g0138 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02976 | hp2 | a0001 | c0001 | t0030 | g0324 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03041 | hp2 | a0001 | c0002 | t0038 | g0301 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03098 | hp1 | a0002 | c0007 | t0043 | g0097 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03098 | hp2 | a0001 | c0006 | t0105 | g0315 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03130 | hp1 | a0001 | c0006 | t0003 | g0219 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03130 | hp2 | a0001 | c0002 | t0008 | g0283 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03139 | hp1 | a0004 | c0009 | t0024 | g0198 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03139 | hp2 | a0002 | c0007 | t0031 | g0316 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03195 | hp1 | a0002 | c0007 | t0044 | g0095 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03195 | hp2 | a0001 | c0006 | t0018 | g0032 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03209 | hp1 | a0001 | c0008 | t0032 | g0086 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03209 | hp2 | a0001 | c0001 | t0069 | g0059 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03225 | hp1 | a0001 | c0002 | t0008 | g0270 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03225 | hp2 | a0001 | c0001 | t0024 | g0307 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03239 | hp1 | a0001 | c0001 | t0019 | g0048 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03239 | hp2 | a0001 | c0001 | t0015 | g0231 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03453 | hp1 | a0002 | c0004 | t0064 | g0223 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03453 | hp2 | a0001 | c0025 | t0028 | g0070 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03490 | hp1 | a0001 | c0002 | t0070 | g0249 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0130 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03491 | hp1 | a0001 | c0002 | t0006 | g0263 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0288 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03516 | hp1 | a0001 | c0011 | t0110 | g0141 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03540 | hp1 | a0001 | c0002 | t0008 | g0237 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03540 | hp2 | a0001 | c0002 | t0108 | g0063 | AFR | GWD | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03579 | hp1 | a0001 | c0005 | t0013 | g0318 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03579 | hp2 | a0001 | c0002 | t0027 | g0305 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03654 | hp1 | a0001 | c0002 | t0005 | g0253 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0195 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0057 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03688 | hp1 | a0015 | c0013 | t0015 | g0036 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0264 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0054 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03831 | hp2 | a0001 | c0002 | t0011 | g0004 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03834 | hp1 | a0001 | c0002 | t0007 | g0124 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03834 | hp2 | a0001 | c0001 | t0014 | g0079 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0021 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03927 | hp2 | a0001 | c0001 | t0100 | g0281 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03942 | hp1 | a0001 | c0001 | t0074 | g0230 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0011 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04115 | hp2 | a0001 | c0002 | t0012 | g0099 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0131 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | BEB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04199 | hp1 | a0001 | c0002 | t0060 | g0261 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04199 | hp2 | a0001 | c0002 | t0107 | g0232 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04204 | hp2 | a0001 | c0001 | t0075 | g0229 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04228 | hp1 | a0001 | c0002 | t0010 | g0203 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18612 | hp2 | a0001 | c0002 | t0004 | g0325 | EAS | CHB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18747 | hp1 | a0001 | c0002 | t0004 | g0248 | EAS | CHB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | YRI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18906 | hp2 | a0004 | c0027 | t0024 | g0215 | AFR | YRI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18942 | hp1 | a0003 | c0003 | t0017 | g0163 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18945 | hp1 | a0001 | c0002 | t0004 | g0268 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18946 | hp2 | a0003 | c0003 | t0017 | g0162 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18947 | hp1 | a0001 | c0002 | t0009 | g0329 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18948 | hp1 | a0001 | c0001 | t0010 | g0187 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18948 | hp2 | a0001 | c0002 | t0009 | g0009 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18949 | hp2 | a0001 | c0002 | t0005 | g0128 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18953 | hp1 | a0001 | c0002 | t0067 | g0170 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18953 | hp2 | a0001 | c0002 | t0022 | g0129 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18954 | hp2 | a0001 | c0001 | t0039 | g0037 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18957 | hp2 | a0001 | c0002 | t0026 | g0117 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18959 | hp2 | a0001 | c0002 | t0056 | g0250 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18960 | hp2 | a0001 | c0001 | t0101 | g0002 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18961 | hp1 | a0001 | c0002 | t0016 | g0126 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18961 | hp2 | a0008 | c0029 | t0002 | g0003 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0113 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18963 | hp2 | a0001 | c0002 | t0021 | g0028 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18969 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18971 | hp2 | a0001 | c0002 | t0009 | g0009 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18979 | hp1 | a0001 | c0001 | t0016 | g0111 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18979 | hp2 | a0001 | c0001 | t0019 | g0192 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18981 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18982 | hp2 | a0001 | c0002 | t0009 | g0031 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18983 | hp1 | a0001 | c0002 | t0041 | g0123 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18983 | hp2 | a0001 | c0002 | t0093 | g0081 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18985 | hp1 | a0001 | c0001 | t0021 | g0193 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18985 | hp2 | a0001 | c0002 | t0045 | g0016 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18987 | hp1 | a0001 | c0001 | t0022 | g0033 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18987 | hp2 | a0001 | c0002 | t0009 | g0260 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18989 | hp1 | a0001 | c0002 | t0061 | g0133 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18990 | hp1 | a0001 | c0002 | t0062 | g0016 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18990 | hp2 | a0003 | c0003 | t0017 | g0185 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18993 | hp1 | a0001 | c0001 | t0015 | g0022 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18995 | hp1 | a0001 | c0001 | t0086 | g0001 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18997 | hp1 | a0001 | c0001 | t0085 | g0206 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18997 | hp2 | a0001 | c0002 | t0009 | g0284 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18998 | hp2 | a0001 | c0001 | t0106 | g0038 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA18999 | hp2 | a0001 | c0002 | t0004 | g0228 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19000 | hp2 | a0001 | c0001 | t0040 | g0213 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19001 | hp2 | a0001 | c0002 | t0025 | g0254 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19007 | hp1 | a0001 | c0002 | t0094 | g0028 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19007 | hp2 | a0001 | c0002 | t0063 | g0196 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19010 | hp1 | a0001 | c0002 | t0098 | g0114 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19011 | hp1 | a0001 | c0002 | t0068 | g0115 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19011 | hp2 | a0001 | c0002 | t0009 | g0221 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19012 | hp1 | a0001 | c0001 | t0087 | g0182 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0226 | AFR | LWK | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19043 | hp2 | a0001 | c0002 | t0008 | g0180 | AFR | LWK | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19054 | hp1 | a0001 | c0001 | t0040 | g0212 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19054 | hp2 | a0001 | c0001 | t0014 | g0186 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19057 | hp2 | a0003 | c0003 | t0037 | g0001 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19058 | hp1 | a0001 | c0002 | t0004 | g0172 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19064 | hp1 | a0001 | c0002 | t0050 | g0103 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19068 | hp1 | a0001 | c0001 | t0036 | g0211 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19068 | hp2 | a0007 | c0016 | t0012 | g0010 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19070 | hp1 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19072 | hp2 | a0001 | c0001 | t0016 | g0120 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19074 | hp1 | a0001 | c0002 | t0059 | g0258 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19074 | hp2 | a0003 | c0003 | t0037 | g0001 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19076 | hp1 | a0001 | c0002 | t0009 | g0031 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19076 | hp2 | a0001 | c0001 | t0099 | g0083 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19077 | hp1 | a0014 | c0015 | t0001 | g0289 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19078 | hp1 | a0001 | c0001 | t0016 | g0109 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19078 | hp2 | a0001 | c0001 | t0039 | g0043 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19079 | hp1 | a0001 | c0002 | t0046 | g0257 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19079 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19081 | hp2 | a0009 | c0024 | t0041 | g0121 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19082 | hp2 | a0001 | c0001 | t0088 | g0202 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19084 | hp1 | a0001 | c0002 | t0009 | g0276 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0112 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19088 | hp1 | a0010 | c0021 | t0079 | g0002 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19088 | hp2 | a0001 | c0002 | t0025 | g0010 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19091 | hp2 | a0001 | c0002 | t0057 | g0071 | EAS | JPT | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | YRI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA19240 | hp2 | a0004 | c0009 | t0051 | g0084 | AFR | YRI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20129 | hp1 | a0002 | c0004 | t0014 | g0136 | AFR | ASW | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20129 | hp2 | a0001 | c0010 | t0072 | g0218 | AFR | ASW | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20752 | hp1 | a0001 | c0001 | t0029 | g0148 | EUR | TSI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0152 | EUR | TSI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20805 | hp1 | a0001 | c0002 | t0007 | g0246 | EUR | TSI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0310 | EUR | TSI | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20905 | hp1 | a0001 | c0001 | t0052 | g0055 | SAS | GIH | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0039 | SAS | GIH | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0207 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02486 | hp1 | a0001 | c0011 | t0109 | g0140 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02486 | hp2 | a0001 | c0001 | t0018 | g0179 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG02559 | hp2 | a0001 | c0006 | t0018 | g0217 | AFR | ACB | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03471 | hp1 | a0001 | c0006 | t0018 | g0330 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG06807 | hp1 | a0001 | c0001 | t0019 | g0093 | AFR | USA | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
HG06807 | hp2 | a0001 | c0002 | t0008 | g0235 | AFR | USA | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | USA | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0205 | AFR | USA | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | LWK | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0004 | g0296 | REF | REF | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0030 | g0092 | REF | REF | ACO1_chr9_32379643_32459769 | ACO1 | chr9 | 32379643 | 32459769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:32384734
|
A | G | 1 | a0001 | 1 | HG04199.hp2 | splice_region_variant | LOW | c.-24A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/21 | chr9 | 32384734 | ||||||
chr9:32405569
|
C | A | 1 | a0015 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.63C>A | p.Phe21Leu | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/21 | 178/7443 | 63/2670 | 21/889 | chr9 | 32405569 | ||
chr9:32407264
|
G | A | 1 | a0006 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.101G>A | p.Arg34His | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/21 | 216/7443 | 101/2670 | 34/889 | chr9 | 32407264 | ||
chr9:32407386
|
G | A | 1 | a0014 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.223G>A | p.Glu75Lys | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/21 | 338/7443 | 223/2670 | 75/889 | chr9 | 32407386 | ||
chr9:32408634
|
G | C | 1 | a0007 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.387G>C | p.Gln129His | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/21 | 502/7443 | 387/2670 | 129/889 | chr9 | 32408634 | ||
chr9:32418421
|
T | C | 1 | a0013 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.568T>C | p.Phe190Leu | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 6/21 | 683/7443 | 568/2670 | 190/889 | chr9 | 32418421 | ||
chr9:32421010
|
C | T | 1 | a0008 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.953C>T | p.Thr318Met | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/21 | 1068/7443 | 953/2670 | 318/889 | chr9 | 32421010 | ||
chr9:32423388
|
A | G | 1 | a0005 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1040A>G | p.Asn347Ser | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/21 | 1155/7443 | 1040/2670 | 347/889 | chr9 | 32423388 | ||
chr9:32423393
|
C | T | 1 | a0012 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1045C>T | p.Pro349Ser | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/21 | 1160/7443 | 1045/2670 | 349/889 | chr9 | 32423393 | ||
chr9:32424661
|
C | A | 1 | a0003 | 8 | HG00673.hp2 HG02074.hp1 HG02132.hp2 others(5): Show |
missense_variant | MODERATE | c.1184C>A | p.Ala395Asp | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/21 | 1299/7443 | 1184/2670 | 395/889 | chr9 | 32424661 | ||
chr9:32427408
|
G | A | 2 | a0002a0013 | 14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
missense_variant | MODERATE | c.1456G>A | p.Gly486Arg | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/21 | 1571/7443 | 1456/2670 | 486/889 | chr9 | 32427408 | ||
chr9:32431730
|
A | C | 1 | a0004 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1738A>C | p.Lys580Gln | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/21 | 1853/7443 | 1738/2670 | 580/889 | chr9 | 32431730 | ||
chr9:32449002
|
C | A | 1 | a0011 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.2477C>A | p.Ala826Asp | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/21 | 2592/7443 | 2477/2670 | 826/889 | chr9 | 32449002 | ||
chr9:32450028
|
A | T | 1 | a0009 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.2587A>T | p.Met863Leu | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2702/7443 | 2587/2670 | 863/889 | chr9 | 32450028 | ||
chr9:32450094
|
C | T | 1 | a0010 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.2653C>T | p.Arg885Cys | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2768/7443 | 2653/2670 | 885/889 | chr9 | 32450094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:32425900
|
T | C | 5 | a0001c0005a0001c0008a0001c0018others(2): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
synonymous_variant | LOW | c.1251T>C | p.Tyr417Tyr | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/21 | 1366/7443 | 1251/2670 | 417/889 | chr9 | 32425900 | ||
chr9:32425912
|
A | G | 12 | a0001c0002a0001c0011a0001c0023others(9): Show | 157 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(154): Show |
synonymous_variant | LOW | c.1263A>G | p.Glu421Glu | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/21 | 1378/7443 | 1263/2670 | 421/889 | chr9 | 32425912 | ||
chr9:32425978
|
G | A | 1 | a0001c0023 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1329G>A | p.Pro443Pro | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/21 | 1444/7443 | 1329/2670 | 443/889 | chr9 | 32425978 | ||
chr9:32427398
|
A | G | 4 | a0001c0005a0001c0006a0001c0008others(1): Show | 16 | HG01243.hp1 HG02280.hp2 HG02559.hp2 others(13): Show |
synonymous_variant | LOW | c.1446A>G | p.Leu482Leu | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/21 | 1561/7443 | 1446/2670 | 482/889 | chr9 | 32427398 | ||
chr9:32448907
|
C | T | 5 | a0001c0008a0001c0010a0001c0022others(2): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
synonymous_variant | LOW | c.2382C>T | p.Ala794Ala | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/21 | 2497/7443 | 2382/2670 | 794/889 | chr9 | 32448907 | ||
chr9:32448961
|
T | G | 7 | a0001c0008a0001c0010a0001c0011others(4): Show | 14 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
synonymous_variant | LOW | c.2436T>G | p.Gly812Gly | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/21 | 2551/7443 | 2436/2670 | 812/889 | chr9 | 32448961 | ||
chr9:32450045
|
T | C | 7 | a0001c0008a0001c0010a0001c0011others(4): Show | 14 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
synonymous_variant | LOW | c.2604T>C | p.Asp868Asp | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2719/7443 | 2604/2670 | 868/889 | chr9 | 32450045 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:32384651
|
A | G | 5 | a0001c0001t0111a0001c0001t0113a0001c0011t0109others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-107A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/21 | 20856 | chr9 | 32384651 | |||||
chr9:32384711
|
C | T | 1 | a0001c0002t0108 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/21 | 20796 | chr9 | 32384711 | |||||
chr9:32450132
|
C | T | 2 | a0001c0002t0041a0009c0024t0041 | 2 | NA18983.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 21 | chr9 | 32450132 | |||||
chr9:32450189
|
T | C | 63 | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(60): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*78T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 78 | chr9 | 32450189 | |||||
chr9:32450226
|
G | A | 2 | a0001c0001t0074a0001c0001t0075 | 2 | HG03942.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 115 | chr9 | 32450226 | |||||
chr9:32450260
|
T | C | 1 | a0001c0019t0112 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 149 | chr9 | 32450260 | |||||
chr9:32450301
|
AATC | A | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*194_*196delATC | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 194 | INFO_REALIGN_3_PRIME | chr9 | 32450301 | ||||
chr9:32450304
|
C | A | 6 | a0001c0011t0109a0001c0011t0110a0002c0007t0031others(3): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*193C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 193 | chr9 | 32450304 | |||||
chr9:32450363
|
A | G | 2 | a0001c0001t0111a0001c0002t0027 | 4 | HG01175.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*252A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 252 | chr9 | 32450363 | |||||
chr9:32450427
|
A | G | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*316A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 316 | chr9 | 32450427 | |||||
chr9:32450430
|
A | AATCTT | 5 | a0001c0001t0029a0001c0001t0033a0001c0001t0076others(2): Show | 8 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*320_*324dupATCTT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 325 | INFO_REALIGN_3_PRIME | chr9 | 32450430 | ||||
chr9:32450517
|
C | T | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*406C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 406 | chr9 | 32450517 | |||||
chr9:32450614
|
C | T | 1 | a0001c0001t0106 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*503C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 503 | chr9 | 32450614 | |||||
chr9:32450735
|
TTTTACTA others(17): Show |
T | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*625_*648delTTTACT others(18): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 625 | chr9 | 32450735 | |||||
chr9:32450739
|
A | ACTAT | 4 | a0001c0001t0080a0001c0002t0008a0005c0012t0008others(1): Show | 13 | HG01496.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*631_*634dupATCT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 635 | INFO_REALIGN_3_PRIME | chr9 | 32450739 | ||||
chr9:32450870
|
TAG | T | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*762_*763delAG | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 762 | INFO_REALIGN_3_PRIME | chr9 | 32450870 | ||||
chr9:32450905
|
A | ACACCATA others(12): Show |
6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*796_*814dupACCATA others(13): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 815 | INFO_REALIGN_3_PRIME | chr9 | 32450905 | ||||
chr9:32450961
|
T | TATCA | 8 | a0001c0002t0013a0001c0002t0034a0001c0002t0082others(5): Show | 12 | HG01255.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*851_*854dupATCA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 855 | INFO_REALIGN_3_PRIME | chr9 | 32450961 | ||||
chr9:32450961
|
T | TATCAATC others(34): Show |
6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*854_*855insATCAGA others(35): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 855 | INFO_REALIGN_3_PRIME | chr9 | 32450961 | ||||
chr9:32450974
|
C | T | 8 | a0001c0002t0070a0001c0002t0071a0001c0008t0032others(5): Show | 9 | HG01192.hp2 HG01243.hp1 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*863C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 863 | chr9 | 32450974 | |||||
chr9:32451013
|
C | T | 2 | a0001c0001t0111a0001c0002t0027 | 4 | HG01175.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*902C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 902 | chr9 | 32451013 | |||||
chr9:32451071
|
T | TA | 11 | a0001c0001t0007a0001c0001t0024a0001c0001t0084others(8): Show | 22 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*962dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 963 | INFO_REALIGN_3_PRIME | chr9 | 32451071 | ||||
chr9:32451146
|
A | G | 96 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(93): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1035A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1035 | chr9 | 32451146 | |||||
chr9:32451434
|
T | A | 1 | a0001c0019t0112 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1323T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1323 | chr9 | 32451434 | |||||
chr9:32451722
|
G | C | 5 | a0001c0001t0011a0001c0002t0011a0001c0002t0048others(2): Show | 9 | HG00323.hp2 HG01106.hp1 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1611G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1611 | chr9 | 32451722 | |||||
chr9:32451801
|
G | T | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1690G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1690 | chr9 | 32451801 | |||||
chr9:32451804
|
T | A | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1693 | chr9 | 32451804 | |||||
chr9:32451811
|
C | A | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1700 | chr9 | 32451811 | |||||
chr9:32451814
|
T | A | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1703T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1703 | chr9 | 32451814 | |||||
chr9:32451815
|
C | A | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1704C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1704 | chr9 | 32451815 | |||||
chr9:32451820
|
T | A | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1709 | chr9 | 32451820 | |||||
chr9:32451822
|
G | C | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1711G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1711 | chr9 | 32451822 | |||||
chr9:32451823
|
G | C | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1712G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1712 | chr9 | 32451823 | |||||
chr9:32451828
|
C | G | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1717C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1717 | chr9 | 32451828 | |||||
chr9:32451828
|
C | T | 1 | a0001c0002t0094 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1717C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1717 | chr9 | 32451828 | |||||
chr9:32451829
|
G | C | 1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1718G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1718 | chr9 | 32451829 | |||||
chr9:32451831
|
G | GTGGCTCA others(15): Show |
1 | a0001c0002t0045 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1720_*1721insTGGC others(18): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1721 | chr9 | 32451831 | |||||
chr9:32451929
|
T | A | 1 | a0001c0002t0050 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1818T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1818 | chr9 | 32451929 | |||||
chr9:32451988
|
C | T | 1 | a0001c0002t0049 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1877C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1877 | chr9 | 32451988 | |||||
chr9:32452064
|
C | CA | 60 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(57): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1968dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1969 | INFO_REALIGN_3_PRIME | chr9 | 32452064 | ||||
chr9:32452096
|
C | T | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1985C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 1985 | chr9 | 32452096 | |||||
chr9:32452169
|
G | A | 4 | a0001c0001t0024a0004c0009t0024a0004c0009t0051others(1): Show | 4 | HG03139.hp1 HG03225.hp2 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2058G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2058 | chr9 | 32452169 | |||||
chr9:32452256
|
G | C | 1 | a0001c0002t0035 | 2 | HG01256.hp2 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2145G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2145 | chr9 | 32452256 | |||||
chr9:32452329
|
C | T | 3 | a0001c0001t0069a0001c0019t0112a0002c0007t0044 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2218C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2218 | chr9 | 32452329 | |||||
chr9:32452342
|
A | G | 14 | a0001c0001t0002a0001c0001t0010a0001c0001t0085others(11): Show | 49 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2231A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2231 | chr9 | 32452342 | |||||
chr9:32452410
|
G | C | 4 | a0001c0001t0016a0001c0001t0087a0001c0001t0088others(1): Show | 7 | HG00280.hp1 NA18961.hp1 NA18979.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2299G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2299 | chr9 | 32452410 | |||||
chr9:32452434
|
T | G | 10 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(7): Show | 11 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2323T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2323 | chr9 | 32452434 | |||||
chr9:32452492
|
G | A | 3 | a0001c0001t0025a0001c0002t0009a0001c0002t0025 | 14 | HG00544.hp1 HG00597.hp1 HG02129.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2381G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2381 | chr9 | 32452492 | |||||
chr9:32452629
|
T | C | 30 | a0001c0001t0006a0001c0001t0015a0001c0001t0022others(27): Show | 54 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2518T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2518 | chr9 | 32452629 | |||||
chr9:32452682
|
C | T | 37 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(34): Show | 115 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2571C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2571 | chr9 | 32452682 | |||||
chr9:32452767
|
C | T | 1 | a0001c0002t0060 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2656C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2656 | chr9 | 32452767 | |||||
chr9:32452794
|
A | T | 86 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(83): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*2683A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2683 | chr9 | 32452794 | |||||
chr9:32452798
|
T | A | 9 | a0001c0001t0020a0001c0001t0033a0001c0001t0076others(6): Show | 18 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2687T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2687 | chr9 | 32452798 | |||||
chr9:32452814
|
T | A | 1 | a0001c0002t0055 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2703T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2703 | chr9 | 32452814 | |||||
chr9:32452898
|
T | A | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2787T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2787 | chr9 | 32452898 | |||||
chr9:32452936
|
A | G | 1 | a0001c0023t0066 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2825A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2825 | chr9 | 32452936 | |||||
chr9:32452938
|
A | G | 1 | a0001c0002t0047 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2827 | chr9 | 32452938 | |||||
chr9:32452939
|
G | A | 1 | a0001c0002t0047 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2828G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2828 | chr9 | 32452939 | |||||
chr9:32452963
|
AC | A | 18 | a0001c0001t0002a0001c0001t0014a0001c0001t0036others(15): Show | 59 | HG00280.hp2 HG00558.hp1 HG00673.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2866delC | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2866 | INFO_REALIGN_3_PRIME | chr9 | 32452963 | ||||
chr9:32452964
|
C | CG | 5 | a0001c0001t0069a0001c0001t0113a0001c0002t0038others(2): Show | 6 | HG02451.hp2 HG02572.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2853_*2854insG | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2854 | chr9 | 32452964 | |||||
chr9:32452965
|
C | G | 37 | a0001c0001t0006a0001c0001t0007a0001c0001t0015others(34): Show | 79 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2854C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2854 | chr9 | 32452965 | |||||
chr9:32452966
|
C | G | 2 | a0001c0002t0058a0001c0002t0059 | 2 | HG02040.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2855C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2855 | chr9 | 32452966 | |||||
chr9:32452972
|
C | T | 1 | a0001c0002t0083 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2861C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2861 | chr9 | 32452972 | |||||
chr9:32452974
|
C | A | 2 | a0001c0001t0111a0001c0002t0027 | 4 | HG01175.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2863C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2863 | chr9 | 32452974 | |||||
chr9:32452975
|
C | A | 7 | a0001c0001t0069a0001c0001t0111a0001c0001t0113others(4): Show | 10 | HG01175.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2864C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2864 | chr9 | 32452975 | |||||
chr9:32452975
|
C | CAA | 3 | a0001c0001t0018a0001c0006t0018a0013c0017t0104 | 6 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2864_*2865insAA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2865 | chr9 | 32452975 | |||||
chr9:32452976
|
C | A | 15 | a0001c0001t0018a0001c0001t0069a0001c0001t0089others(12): Show | 21 | HG01175.hp2 HG01891.hp2 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2865C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2865 | chr9 | 32452976 | |||||
chr9:32452976
|
C | CAA | 18 | a0001c0001t0006a0001c0001t0022a0001c0001t0024others(15): Show | 43 | HG00597.hp2 HG00741.hp1 HG01069.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2865_*2866insAA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2866 | chr9 | 32452976 | |||||
chr9:32452977
|
C | A | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*2866C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2866 | chr9 | 32452977 | |||||
chr9:32452977
|
C | CA | 28 | a0001c0001t0005a0001c0001t0025a0001c0001t0033others(25): Show | 46 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2876dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2877 | INFO_REALIGN_3_PRIME | chr9 | 32452977 | ||||
chr9:32452977
|
C | CAAA | 11 | a0001c0001t0007a0001c0001t0015a0001c0001t0074others(8): Show | 25 | HG00323.hp1 HG00733.hp1 HG01099.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2874_*2876dupAAA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2877 | INFO_REALIGN_3_PRIME | chr9 | 32452977 | ||||
chr9:32452989
|
T | C | 2 | a0001c0002t0056a0001c0002t0057 | 2 | NA18959.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2878T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2878 | chr9 | 32452989 | |||||
chr9:32453071
|
G | A | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2960G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 2960 | chr9 | 32453071 | |||||
chr9:32453121
|
C | G | 98 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(95): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*3010C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3010 | chr9 | 32453121 | |||||
chr9:32453135
|
CCT | C | 39 | a0001c0001t0006a0001c0001t0015a0001c0001t0018others(36): Show | 64 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3025_*3026delCT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3025 | chr9 | 32453135 | |||||
chr9:32453175
|
C | T | 1 | a0001c0022t0073 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3064C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3064 | chr9 | 32453175 | |||||
chr9:32453179
|
G | A | 2 | a0001c0010t0072a0001c0022t0073 | 2 | HG01192.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3068G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3068 | chr9 | 32453179 | |||||
chr9:32453197
|
G | GAGTT | 3 | a0001c0001t0018a0001c0006t0018a0001c0006t0105 | 6 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3092_*3095dupGTTA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3096 | INFO_REALIGN_3_PRIME | chr9 | 32453197 | ||||
chr9:32453201
|
T | A | 3 | a0001c0002t0050a0003c0003t0017a0003c0003t0037 | 8 | HG00673.hp2 HG02132.hp2 NA18942.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3090T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3090 | chr9 | 32453201 | |||||
chr9:32453280
|
T | C | 33 | a0001c0001t0004a0001c0001t0011a0001c0001t0025others(30): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3169T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3169 | chr9 | 32453280 | |||||
chr9:32453357
|
G | GA | 123 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(120): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*3260dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3261 | INFO_REALIGN_3_PRIME | chr9 | 32453357 | ||||
chr9:32453357
|
G | GAA | 9 | a0001c0001t0007a0001c0001t0084a0001c0001t0092others(6): Show | 20 | HG00733.hp1 HG01070.hp1 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3259_*3260dupAA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3261 | INFO_REALIGN_3_PRIME | chr9 | 32453357 | ||||
chr9:32453379
|
C | T | 5 | a0001c0001t0022a0001c0001t0099a0001c0001t0101others(2): Show | 7 | NA18953.hp2 NA18960.hp2 NA18981.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3268C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3268 | chr9 | 32453379 | |||||
chr9:32453434
|
C | G | 6 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(3): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3323C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 3323 | chr9 | 32453434 | |||||
chr9:32454138
|
C | G | 1 | a0001c0002t0059 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4027C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4027 | chr9 | 32454138 | |||||
chr9:32454172
|
G | A | 1 | a0001c0002t0065 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4061G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4061 | chr9 | 32454172 | |||||
chr9:32454185
|
T | C | 1 | a0001c0023t0066 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4074T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4074 | chr9 | 32454185 | |||||
chr9:32454208
|
C | T | 7 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(4): Show | 8 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4097C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4097 | chr9 | 32454208 | |||||
chr9:32454273
|
CACGCACT others(21): Show |
C | 1 | a0001c0002t0068 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4164_*4191delCGCA others(24): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4164 | INFO_REALIGN_3_PRIME | chr9 | 32454273 | ||||
chr9:32454298
|
C | T | 1 | a0001c0002t0093 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4187C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4187 | chr9 | 32454298 | |||||
chr9:32454307
|
C | T | 2 | a0001c0001t0111a0001c0002t0027 | 4 | HG01175.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4196C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4196 | chr9 | 32454307 | |||||
chr9:32454350
|
T | A | 6 | a0001c0001t0007a0001c0001t0084a0001c0001t0111others(3): Show | 17 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4239T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4239 | chr9 | 32454350 | |||||
chr9:32454370
|
GA | G | 22 | a0001c0001t0006a0001c0001t0015a0001c0001t0022others(19): Show | 41 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4261delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4261 | INFO_REALIGN_3_PRIME | chr9 | 32454370 | ||||
chr9:32454451
|
A | G | 7 | a0001c0008t0032a0001c0010t0028a0001c0010t0072others(4): Show | 8 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4340A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4340 | chr9 | 32454451 | |||||
chr9:32454457
|
ATAACAAG others(12): Show |
A | 6 | a0001c0001t0069a0001c0001t0080a0001c0001t0113others(3): Show | 7 | HG02451.hp2 HG02572.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4352_*4370delAGGT others(15): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4352 | INFO_REALIGN_3_PRIME | chr9 | 32454457 | ||||
chr9:32454559
|
T | C | 2 | a0001c0001t0111a0001c0002t0027 | 4 | HG01175.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4448T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4448 | chr9 | 32454559 | |||||
chr9:32454667
|
T | C | 1 | a0001c0023t0066 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4556T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 21/21 | 4556 | chr9 | 32454667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:32384827
|
G | A | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+92G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32384827 | ||||||
chr9:32384828
|
C | A | 1 | a0001c0001t0076g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-23+93C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32384828 | ||||||
chr9:32384845
|
A | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(262): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23+110A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32384845 | ||||||
chr9:32384935
|
A | G | 1 | a0001c0002t0002g0142 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-23+200A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32384935 | ||||||
chr9:32385122
|
C | A | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-23+387C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385122 | ||||||
chr9:32385374
|
A | T | 1 | a0001c0002t0010g0332 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-23+639A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385374 | ||||||
chr9:32385457
|
A | T | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-23+722A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385457 | ||||||
chr9:32385498
|
T | A | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-23+763T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385498 | ||||||
chr9:32385595
|
A | T | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-23+860A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385595 | ||||||
chr9:32385698
|
G | A | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-23+963G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385698 | ||||||
chr9:32385833
|
C | T | 8 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+1098C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385833 | ||||||
chr9:32385851
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(278): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-23+1116G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32385851 | ||||||
chr9:32386067
|
A | T | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-23+1332A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386067 | ||||||
chr9:32386068
|
C | T | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0002t0004g0069others(3): Show | 6 | HG01256.hp2 HG01346.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+1333C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386068 | ||||||
chr9:32386150
|
G | T | 1 | a0001c0001t0076g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-23+1415G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386150 | ||||||
chr9:32386347
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23+1612C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386347 | ||||||
chr9:32386439
|
G | A | 8 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+1704G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386439 | ||||||
chr9:32386477
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(96): Show | 108 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-23+1742G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386477 | ||||||
chr9:32386519
|
T | C | 1 | a0001c0002t0057g0071 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-23+1784T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386519 | ||||||
chr9:32386648
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-23+1913G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386648 | ||||||
chr9:32386711
|
G | A | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+1976G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386711 | ||||||
chr9:32386825
|
G | T | 2 | a0001c0006t0018g0032a0001c0006t0018g0330 | 3 | HG02280.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-23+2090G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386825 | ||||||
chr9:32386840
|
C | T | 1 | a0001c0002t0011g0060 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-23+2105C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386840 | ||||||
chr9:32386841
|
G | A | 3 | a0001c0006t0003g0219a0001c0006t0018g0217a0001c0010t0072g0218 | 3 | HG02559.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-23+2106G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32386841 | ||||||
chr9:32387000
|
C | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+2265C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387000 | ||||||
chr9:32387061
|
T | C | 35 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(32): Show | 38 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-23+2326T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387061 | ||||||
chr9:32387123
|
T | G | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23+2388T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387123 | ||||||
chr9:32387411
|
C | G | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23+2676C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387411 | ||||||
chr9:32387523
|
G | T | 1 | a0001c0001t0092g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-23+2788G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387523 | ||||||
chr9:32387684
|
A | C | 137 | a0001c0001t0001g0067a0001c0001t0001g0238a0001c0001t0001g0265others(134): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-23+2949A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387684 | ||||||
chr9:32387930
|
C | T | 1 | a0004c0027t0024g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-23+3195C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387930 | ||||||
chr9:32387947
|
T | G | 5 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0002t0004g0069others(2): Show | 5 | HG01256.hp2 HG01346.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+3212T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32387947 | ||||||
chr9:32388076
|
T | A | 14 | a0001c0001t0001g0151a0001c0001t0002g0149a0001c0001t0006g0152others(11): Show | 14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-23+3341T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388076 | ||||||
chr9:32388171
|
T | G | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23+3436T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388171 | ||||||
chr9:32388195
|
C | G | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23+3460C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388195 | ||||||
chr9:32388256
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0005g0155a0001c0001t0005g0156 | 3 | HG02602.hp1 NA18989.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-23+3521G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388256 | ||||||
chr9:32388309
|
G | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0080others(19): Show | 23 | HG01074.hp1 HG01109.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-23+3574G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388309 | ||||||
chr9:32388401
|
G | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0329 | 3 | NA18947.hp1 NA18982.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-23+3666G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388401 | ||||||
chr9:32388839
|
G | T | 8 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+4104G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388839 | ||||||
chr9:32388922
|
C | T | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23+4187C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388922 | ||||||
chr9:32388941
|
G | A | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+4206G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388941 | ||||||
chr9:32388991
|
A | G | 1 | a0001c0025t0028g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-23+4256A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32388991 | ||||||
chr9:32389015
|
A | C | 1 | a0001c0001t0006g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-23+4280A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389015 | ||||||
chr9:32389028
|
A | G | 13 | a0001c0001t0001g0053a0001c0001t0003g0005a0001c0001t0003g0051others(10): Show | 15 | HG00741.hp1 HG01261.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.-23+4293A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389028 | ||||||
chr9:32389050
|
G | C | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-23+4315G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389050 | ||||||
chr9:32389233
|
C | T | 5 | a0001c0001t0003g0210a0001c0001t0003g0214a0001c0001t0036g0211others(2): Show | 5 | NA19000.hp2 NA19054.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+4498C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389233 | ||||||
chr9:32389400
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(97): Show | 109 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-23+4665C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389400 | ||||||
chr9:32389451
|
C | G | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0002t0004g0069others(3): Show | 6 | HG01256.hp2 HG01346.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+4716C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389451 | ||||||
chr9:32389465
|
G | A | 129 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(126): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-23+4730G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389465 | ||||||
chr9:32389669
|
C | CT | 94 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(91): Show | 102 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-23+4949dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32389669 | |||||
chr9:32389669
|
CT | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0072others(163): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-23+4949delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32389669 | |||||
chr9:32389757
|
C | T | 1 | a0001c0008t0032g0326 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-23+5022C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389757 | ||||||
chr9:32389772
|
A | G | 42 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0108others(39): Show | 45 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23+5037A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389772 | ||||||
chr9:32389800
|
C | CT | 83 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(80): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-23+5081dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32389800 | |||||
chr9:32389800
|
C | CTT | 145 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(142): Show | 157 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.-23+5080_-23+5081d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32389800 | |||||
chr9:32389800
|
C | CTTT | 91 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(88): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.-23+5079_-23+5081d others(5): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32389800 | |||||
chr9:32389800
|
C | CTTTT | 29 | a0001c0001t0001g0308a0001c0001t0002g0322a0001c0001t0004g0310others(26): Show | 32 | HG00733.hp1 HG01175.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-23+5078_-23+5081d others(6): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32389800 | |||||
chr9:32389800
|
C | T | 1 | a0001c0002t0004g0325 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-23+5065C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389800 | ||||||
chr9:32389843
|
G | A | 1 | a0001c0006t0018g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-23+5108G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389843 | ||||||
chr9:32389943
|
G | A | 1 | a0001c0006t0018g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-23+5208G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32389943 | ||||||
chr9:32390076
|
G | T | 1 | a0001c0001t0030g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-23+5341G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390076 | ||||||
chr9:32390079
|
T | A | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-23+5344T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390079 | ||||||
chr9:32390163
|
G | C | 1 | a0001c0001t0019g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-23+5428G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390163 | ||||||
chr9:32390188
|
A | T | 2 | a0001c0002t0013g0064a0001c0002t0038g0328 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+5453A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390188 | ||||||
chr9:32390208
|
A | T | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23+5473A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390208 | ||||||
chr9:32390284
|
G | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(301): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-23+5549G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390284 | ||||||
chr9:32390304
|
C | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-23+5569C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390304 | ||||||
chr9:32390336
|
C | T | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+5601C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390336 | ||||||
chr9:32390353
|
A | G | 28 | a0001c0001t0001g0308a0001c0001t0002g0322a0001c0001t0004g0310others(25): Show | 31 | HG00733.hp1 HG01175.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+5618A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390353 | ||||||
chr9:32390375
|
G | A | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23+5640G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390375 | ||||||
chr9:32390475
|
A | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(48): Show | 55 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.-23+5740A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390475 | ||||||
chr9:32390478
|
CT | C | 3 | a0001c0001t0029g0017a0001c0001t0077g0017a0001c0002t0002g0144 | 3 | HG00639.hp1 HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-23+5744delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390478 | ||||||
chr9:32390493
|
C | T | 1 | a0001c0001t0014g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-23+5758C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390493 | ||||||
chr9:32390582
|
A | G | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+5847A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390582 | ||||||
chr9:32390750
|
G | C | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23+6015G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390750 | ||||||
chr9:32390800
|
A | T | 5 | a0001c0001t0003g0007a0001c0001t0003g0161a0001c0001t0019g0007others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+6065A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390800 | ||||||
chr9:32390939
|
C | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(301): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-23+6204C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32390939 | ||||||
chr9:32391018
|
A | G | 2 | a0001c0002t0013g0064a0001c0002t0038g0328 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+6283A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32391018 | ||||||
chr9:32391138
|
G | A | 1 | a0001c0002t0004g0228 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-23+6403G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32391138 | ||||||
chr9:32391444
|
C | T | 5 | a0001c0001t0004g0297a0001c0002t0004g0296a0001c0002t0011g0004others(2): Show | 8 | HG00140.hp2 HG00323.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23+6709C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32391444 | ||||||
chr9:32391739
|
C | A | 1 | a0001c0001t0020g0327 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-23+7004C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32391739 | ||||||
chr9:32391786
|
C | G | 123 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(120): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-23+7051C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32391786 | ||||||
chr9:32391811
|
CAGATA | C | 3 | a0001c0002t0008g0302a0001c0002t0038g0301a0001c0002t0083g0300 | 3 | HG02647.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-23+7083_-23+7087d others(7): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32391811 | |||||
chr9:32391940
|
TTA | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0080others(19): Show | 23 | HG01074.hp1 HG01109.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-23+7207_-23+7208d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32391940 | |||||
chr9:32392181
|
G | A | 42 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0108others(39): Show | 45 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23+7446G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392181 | ||||||
chr9:32392326
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(98): Show | 110 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-23+7591G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392326 | ||||||
chr9:32392431
|
A | G | 123 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(120): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-23+7696A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392431 | ||||||
chr9:32392574
|
G | A | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23+7839G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392574 | ||||||
chr9:32392599
|
C | T | 3 | a0001c0002t0008g0302a0001c0002t0038g0301a0001c0002t0083g0300 | 3 | HG02647.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-23+7864C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392599 | ||||||
chr9:32392613
|
A | G | 123 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(120): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-23+7878A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392613 | ||||||
chr9:32392654
|
C | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+7919C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392654 | ||||||
chr9:32392747
|
G | A | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+8012G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392747 | ||||||
chr9:32392799
|
G | A | 1 | a0001c0001t0087g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-23+8064G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392799 | ||||||
chr9:32392871
|
A | G | 14 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0002t0004g0069others(11): Show | 14 | HG01256.hp2 HG01346.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+8136A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392871 | ||||||
chr9:32392921
|
A | G | 1 | a0001c0001t0080g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-23+8186A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392921 | ||||||
chr9:32392956
|
C | T | 1 | a0001c0001t0102g0295 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-23+8221C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392956 | ||||||
chr9:32392987
|
G | A | 92 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(89): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-23+8252G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32392987 | ||||||
chr9:32393088
|
G | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(301): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-23+8353G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393088 | ||||||
chr9:32393165
|
G | A | 1 | a0001c0002t0001g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-23+8430G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393165 | ||||||
chr9:32393198
|
T | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(301): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-23+8463T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393198 | ||||||
chr9:32393216
|
T | C | 1 | a0001c0001t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-23+8481T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393216 | ||||||
chr9:32393320
|
G | A | 1 | a0001c0001t0004g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-23+8585G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393320 | ||||||
chr9:32393330
|
G | A | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+8595G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393330 | ||||||
chr9:32393382
|
C | T | 3 | a0001c0001t0001g0024a0001c0011t0109g0140a0001c0011t0110g0141 | 4 | HG02486.hp1 HG03516.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+8647C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393382 | ||||||
chr9:32393417
|
C | T | 2 | a0001c0002t0002g0293a0001c0002t0002g0294 | 2 | HG01167.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-23+8682C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393417 | ||||||
chr9:32393527
|
C | A | 5 | a0001c0001t0015g0231a0001c0001t0074g0230a0001c0001t0075g0229others(2): Show | 5 | HG00323.hp1 HG03239.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+8792C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393527 | ||||||
chr9:32393535
|
G | C | 1 | a0001c0002t0002g0224 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-23+8800G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393535 | ||||||
chr9:32393541
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-23+8806A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393541 | ||||||
chr9:32393568
|
G | T | 1 | a0002c0004t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+8833G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393568 | ||||||
chr9:32393718
|
G | A | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+8983G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393718 | ||||||
chr9:32393751
|
C | T | 2 | a0001c0001t0006g0291a0001c0001t0006g0292 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-23+9016C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393751 | ||||||
chr9:32393811
|
A | G | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+9076A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393811 | ||||||
chr9:32393941
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0002t0004g0069others(5): Show | 8 | HG01256.hp2 HG01346.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23+9206G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32393941 | ||||||
chr9:32394172
|
C | A | 3 | a0001c0001t0033g0145a0001c0001t0033g0147a0001c0001t0078g0146 | 3 | HG00741.hp2 HG01433.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-23+9437C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394172 | ||||||
chr9:32394300
|
G | T | 2 | a0001c0001t0002g0322a0001c0001t0015g0321 | 2 | HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-23+9565G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394300 | ||||||
chr9:32394424
|
C | T | 159 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(156): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-23+9689C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394424 | ||||||
chr9:32394491
|
G | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-23+9756G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394491 | ||||||
chr9:32394504
|
G | C | 2 | a0001c0001t0006g0291a0001c0001t0006g0292 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-23+9769G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394504 | ||||||
chr9:32394526
|
CTTTAGTA | C | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+9795_-23+9801d others(9): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32394526 | |||||
chr9:32394721
|
C | T | 2 | a0001c0002t0012g0290a0001c0002t0108g0063 | 2 | HG00735.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-23+9986C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394721 | ||||||
chr9:32394783
|
A | T | 123 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(120): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-23+10048A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394783 | ||||||
chr9:32394788
|
A | G | 159 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(156): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-23+10053A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394788 | ||||||
chr9:32394839
|
A | C | 17 | a0001c0001t0002g0322a0001c0001t0004g0310a0001c0001t0007g0030others(14): Show | 19 | HG00733.hp1 HG01175.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-23+10104A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394839 | ||||||
chr9:32394842
|
A | G | 1 | a0001c0002t0008g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-23+10107A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394842 | ||||||
chr9:32394945
|
G | GC | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+10213dupC | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32394945 | |||||
chr9:32394948
|
C | CT | 263 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(260): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-23+10213_-23+1021 others(5): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394948 | ||||||
chr9:32394950
|
G | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(262): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23+10215G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32394950 | ||||||
chr9:32395015
|
C | T | 123 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(120): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-23+10280C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395015 | ||||||
chr9:32395046
|
A | G | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+10311A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395046 | ||||||
chr9:32395065
|
C | T | 1 | a0014c0015t0001g0289 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-23+10330C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395065 | ||||||
chr9:32395082
|
C | G | 35 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(32): Show | 38 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-23+10347C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395082 | ||||||
chr9:32395101
|
T | C | 1 | a0001c0001t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-23+10366T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395101 | ||||||
chr9:32395128
|
A | G | 123 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(120): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-22-10357A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395128 | ||||||
chr9:32395177
|
C | A | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-10308C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395177 | ||||||
chr9:32395203
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(279): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-22-10282T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395203 | ||||||
chr9:32395204
|
G | A | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-10281G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395204 | ||||||
chr9:32395250
|
C | T | 5 | a0001c0001t0006g0130a0001c0001t0006g0131a0001c0002t0108g0063others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-10235C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395250 | ||||||
chr9:32395345
|
G | T | 2 | a0001c0001t0006g0288a0001c0002t0004g0287 | 2 | HG01099.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-22-10140G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395345 | ||||||
chr9:32395404
|
G | A | 346 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(343): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-22-10081G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395404 | ||||||
chr9:32395432
|
C | T | 1 | a0001c0001t0007g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-22-10053C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395432 | ||||||
chr9:32395475
|
C | CA | 265 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(262): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-22-10004dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32395475 | |||||
chr9:32395776
|
G | A | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-9709G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395776 | ||||||
chr9:32395843
|
A | G | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-9642A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395843 | ||||||
chr9:32395882
|
C | T | 1 | a0001c0002t0002g0286 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-22-9603C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395882 | ||||||
chr9:32395898
|
G | A | 92 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(89): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-22-9587G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395898 | ||||||
chr9:32395922
|
G | A | 1 | a0001c0002t0012g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-22-9563G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32395922 | ||||||
chr9:32396248
|
A | G | 1 | a0001c0001t0080g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22-9237A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396248 | ||||||
chr9:32396412
|
A | G | 1 | a0001c0002t0013g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-22-9073A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396412 | ||||||
chr9:32396508
|
G | A | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0006t0003g0219others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-8977G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396508 | ||||||
chr9:32396532
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0010t0028g0066 | 3 | HG02280.hp1 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-22-8953G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396532 | ||||||
chr9:32396554
|
ACGTGAGG others(4): Show |
A | 1 | a0001c0001t0092g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-22-8929_-22-8919d others(13): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32396554 | |||||
chr9:32396647
|
ACTGCTTT others(4): Show |
A | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(98): Show | 110 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22-8830_-22-8820d others(13): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32396647 | |||||
chr9:32396657
|
C | T | 2 | a0001c0002t0013g0064a0001c0002t0038g0328 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-8828C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396657 | ||||||
chr9:32396728
|
C | G | 1 | a0001c0002t0027g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-22-8757C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396728 | ||||||
chr9:32396742
|
A | G | 1 | a0013c0017t0104g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22-8743A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396742 | ||||||
chr9:32396764
|
G | A | 2 | a0001c0002t0002g0293a0001c0002t0002g0294 | 2 | HG01167.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-22-8721G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396764 | ||||||
chr9:32396988
|
A | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(268): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-22-8497A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32396988 | ||||||
chr9:32397012
|
A | G | 1 | a0001c0001t0018g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-22-8473A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397012 | ||||||
chr9:32397262
|
C | A | 1 | a0001c0001t0011g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22-8223C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397262 | ||||||
chr9:32397284
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(252): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-22-8201G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397284 | ||||||
chr9:32397306
|
T | C | 5 | a0001c0001t0006g0011a0001c0001t0006g0034a0001c0001t0015g0035others(2): Show | 5 | HG01070.hp1 HG02698.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-8179T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397306 | ||||||
chr9:32397644
|
C | T | 10 | a0001c0001t0030g0324a0001c0002t0082g0320a0001c0005t0013g0317others(7): Show | 11 | HG01255.hp1 HG02280.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22-7841C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397644 | ||||||
chr9:32397831
|
C | T | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-22-7654C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397831 | ||||||
chr9:32397922
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(98): Show | 110 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22-7563C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397922 | ||||||
chr9:32397929
|
G | C | 2 | a0001c0002t0013g0064a0001c0002t0038g0328 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-7556G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32397929 | ||||||
chr9:32398037
|
G | C | 3 | a0001c0002t0108g0063a0002c0004t0023g0008a0002c0004t0064g0223 | 5 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-7448G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398037 | ||||||
chr9:32398162
|
A | G | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-7323A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398162 | ||||||
chr9:32398188
|
A | G | 1 | a0003c0003t0004g0209 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-22-7297A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398188 | ||||||
chr9:32398234
|
A | T | 1 | a0001c0001t0019g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-22-7251A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398234 | ||||||
chr9:32398236
|
G | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(264): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-22-7249G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398236 | ||||||
chr9:32398252
|
T | C | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-7233T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398252 | ||||||
chr9:32398490
|
T | C | 2 | a0001c0001t0006g0130a0001c0001t0006g0131 | 2 | HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-22-6995T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398490 | ||||||
chr9:32398540
|
CT | C | 16 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0002t0027g0303others(13): Show | 17 | HG01175.hp2 HG01243.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-22-6934delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32398540 | |||||
chr9:32398557
|
T | G | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-6928T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398557 | ||||||
chr9:32398577
|
G | GT | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-22-6899dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32398577 | |||||
chr9:32398577
|
GTT | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(98): Show | 110 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22-6900_-22-6899d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32398577 | |||||
chr9:32398585
|
T | C | 4 | a0001c0005t0081g0314a0001c0006t0018g0032a0001c0006t0018g0330others(1): Show | 5 | HG02280.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-6900T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398585 | ||||||
chr9:32398595
|
G | A | 1 | a0001c0001t0036g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-22-6890G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398595 | ||||||
chr9:32398692
|
C | T | 35 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(32): Show | 38 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-22-6793C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398692 | ||||||
chr9:32398792
|
G | A | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-6693G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398792 | ||||||
chr9:32398795
|
A | T | 2 | a0001c0002t0004g0069a0001c0002t0035g0068 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-22-6690A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398795 | ||||||
chr9:32398800
|
G | T | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-6685G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398800 | ||||||
chr9:32398843
|
C | T | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-6642C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398843 | ||||||
chr9:32398915
|
T | C | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0006t0003g0219others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-6570T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32398915 | ||||||
chr9:32399286
|
C | G | 1 | a0001c0001t0069g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-22-6199C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399286 | ||||||
chr9:32399381
|
A | T | 1 | a0001c0002t0008g0285 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-22-6104A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399381 | ||||||
chr9:32399473
|
G | A | 4 | a0001c0002t0108g0063a0002c0004t0001g0135a0002c0004t0001g0137others(1): Show | 4 | HG02922.hp2 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-6012G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399473 | ||||||
chr9:32399516
|
A | G | 8 | a0001c0001t0001g0308a0001c0001t0080g0323a0001c0002t0027g0303others(5): Show | 9 | HG01175.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-5969A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399516 | ||||||
chr9:32399593
|
C | T | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-5892C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399593 | ||||||
chr9:32399677
|
T | C | 1 | a0001c0001t0040g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-22-5808T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399677 | ||||||
chr9:32399738
|
C | T | 4 | a0001c0002t0013g0064a0001c0002t0038g0328a0002c0004t0023g0008others(1): Show | 6 | HG01070.hp2 HG01071.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-5747C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399738 | ||||||
chr9:32399807
|
A | AT | 150 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(147): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.-22-5666dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399807 | |||||
chr9:32399912
|
A | ATTTTCTG others(3): Show |
1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5570_-22-5561d others(12): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399912 | |||||
chr9:32399934
|
A | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5551A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399934 | ||||||
chr9:32399935
|
G | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5550G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399935 | ||||||
chr9:32399936
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5549C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399936 | ||||||
chr9:32399937
|
A | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5548A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399937 | ||||||
chr9:32399939
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5546C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399939 | ||||||
chr9:32399941
|
A | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5544A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399941 | ||||||
chr9:32399945
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5540C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399945 | ||||||
chr9:32399950
|
A | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5535A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399950 | ||||||
chr9:32399958
|
C | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0234 | 2 | NA19057.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-22-5527C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399958 | ||||||
chr9:32399964
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5521C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399964 | ||||||
chr9:32399966
|
G | GT | 25 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0080others(22): Show | 27 | HG00733.hp1 HG01074.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-22-5497dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399966
|
G | GTT | 28 | a0001c0001t0001g0067a0001c0001t0003g0056a0001c0001t0003g0065others(25): Show | 29 | HG01175.hp1 HG01981.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22-5498_-22-5497d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399966
|
G | GTTT | 21 | a0001c0001t0001g0238a0001c0001t0001g0308a0001c0001t0014g0226others(18): Show | 22 | HG00323.hp1 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22-5499_-22-5497d others(5): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399966
|
G | GTTTT | 60 | a0001c0001t0001g0265a0001c0001t0004g0297a0001c0001t0005g0239others(57): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-22-5500_-22-5497d others(6): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399966
|
G | GTTTTT | 25 | a0001c0001t0001g0278a0001c0001t0001g0282a0001c0001t0006g0292others(22): Show | 25 | HG00597.hp1 HG00738.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22-5501_-22-5497d others(7): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399966
|
G | T | 1 | a0001c0002t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22-5519G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399966 | ||||||
chr9:32399966
|
GT | G | 61 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0108others(58): Show | 64 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-22-5497delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399966
|
GTT | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(79): Show | 91 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-22-5498_-22-5497d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32399966 | |||||
chr9:32399972
|
T | TG | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(29): Show | 35 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-22-5513_-22-5512i others(3): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32399972 | ||||||
chr9:32400001
|
C | T | 1 | a0001c0002t0008g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-22-5484C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400001 | ||||||
chr9:32400102
|
C | G | 1 | a0001c0006t0003g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-22-5383C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400102 | ||||||
chr9:32400131
|
C | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22-5354C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400131 | ||||||
chr9:32400223
|
G | A | 2 | a0002c0007t0031g0094a0002c0007t0044g0095 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-22-5262G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400223 | ||||||
chr9:32400223
|
G | C | 2 | a0001c0002t0011g0060a0001c0002t0049g0050 | 2 | HG01981.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-22-5262G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400223 | ||||||
chr9:32400250
|
T | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(271): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-22-5235T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400250 | ||||||
chr9:32400253
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(301): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-22-5232A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400253 | ||||||
chr9:32400502
|
G | A | 1 | a0001c0002t0010g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-22-4983G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400502 | ||||||
chr9:32400766
|
A | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-22-4719A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400766 | ||||||
chr9:32400834
|
A | G | 1 | a0001c0002t0002g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-22-4651A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400834 | ||||||
chr9:32400905
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-4580A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400905 | ||||||
chr9:32400947
|
GT | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(271): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-22-4524delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32400947 | |||||
chr9:32400951
|
T | G | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0006t0003g0219others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-4534T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400951 | ||||||
chr9:32400978
|
T | C | 1 | a0001c0001t0005g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-4507T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32400978 | ||||||
chr9:32401032
|
T | C | 116 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(113): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-4453T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401032 | ||||||
chr9:32401074
|
G | A | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-22-4411G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401074 | ||||||
chr9:32401088
|
A | G | 3 | a0001c0002t0008g0302a0001c0002t0038g0301a0001c0002t0083g0300 | 3 | HG02647.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-22-4397A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401088 | ||||||
chr9:32401179
|
G | A | 3 | a0001c0001t0033g0145a0001c0001t0033g0147a0001c0001t0078g0146 | 3 | HG00741.hp2 HG01433.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-22-4306G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401179 | ||||||
chr9:32401193
|
TA | T | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-4291delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401193 | ||||||
chr9:32401332
|
G | GT | 7 | a0001c0001t0001g0119a0001c0001t0016g0120a0001c0001t0022g0033others(4): Show | 7 | HG01515.hp1 NA18956.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-4143dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32401332 | |||||
chr9:32401332
|
GT | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(46): Show | 53 | HG00558.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-22-4143delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32401332 | |||||
chr9:32401388
|
A | AT | 8 | a0001c0001t0001g0238a0001c0001t0007g0271a0001c0001t0014g0226others(5): Show | 9 | HG01099.hp1 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-4084dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32401388 | |||||
chr9:32401408
|
A | C | 351 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(348): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.-22-4077A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401408 | ||||||
chr9:32401598
|
G | T | 1 | a0001c0002t0007g0269 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-22-3887G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401598 | ||||||
chr9:32401612
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(214): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-22-3873A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401612 | ||||||
chr9:32401725
|
C | T | 91 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(88): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.-22-3760C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401725 | ||||||
chr9:32401813
|
C | T | 4 | a0001c0002t0045g0016a0001c0002t0057g0071a0001c0002t0061g0133others(1): Show | 4 | NA18985.hp2 NA18989.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-3672C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401813 | ||||||
chr9:32401971
|
T | G | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-22-3514T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401971 | ||||||
chr9:32401980
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0080others(27): Show | 32 | HG00733.hp1 HG01074.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-22-3505G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32401980 | ||||||
chr9:32402134
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-22-3351T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402134 | ||||||
chr9:32402256
|
A | G | 2 | a0001c0006t0018g0032a0001c0006t0018g0330 | 3 | HG02280.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-22-3229A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402256 | ||||||
chr9:32402275
|
C | G | 1 | a0001c0002t0004g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-22-3210C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402275 | ||||||
chr9:32402422
|
A | G | 5 | a0001c0001t0003g0177a0001c0002t0013g0064a0001c0002t0038g0328others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-3063A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402422 | ||||||
chr9:32402656
|
T | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(271): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-22-2829T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402656 | ||||||
chr9:32402763
|
G | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(256): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-22-2722G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402763 | ||||||
chr9:32402888
|
T | A | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-22-2597T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32402888 | ||||||
chr9:32403072
|
C | T | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-2413C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403072 | ||||||
chr9:32403097
|
A | C | 1 | a0001c0001t0004g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-22-2388A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403097 | ||||||
chr9:32403209
|
G | A | 1 | a0001c0001t0006g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-22-2276G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403209 | ||||||
chr9:32403292
|
C | T | 91 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(88): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.-22-2193C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403292 | ||||||
chr9:32403426
|
G | A | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-2059G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403426 | ||||||
chr9:32403622
|
A | G | 1 | a0001c0002t0004g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-22-1863A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403622 | ||||||
chr9:32403635
|
A | G | 1 | a0001c0002t0004g0227 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-22-1850A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403635 | ||||||
chr9:32403737
|
T | A | 1 | a0001c0025t0028g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-1748T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403737 | ||||||
chr9:32403780
|
G | A | 1 | a0001c0001t0102g0295 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-22-1705G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403780 | ||||||
chr9:32403791
|
C | T | 1 | a0001c0001t0006g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-22-1694C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403791 | ||||||
chr9:32403915
|
T | TGGGGAGT others(23): Show |
4 | a0001c0002t0013g0064a0001c0002t0038g0328a0002c0004t0023g0008others(1): Show | 6 | HG01070.hp2 HG01071.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-1567_-22-1538d others(32): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr9 | 32403915 | |||||
chr9:32403917
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-22-1568G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403917 | ||||||
chr9:32403934
|
G | A | 3 | a0001c0001t0001g0101a0001c0002t0002g0100a0001c0002t0002g0102 | 3 | NA18970.hp2 NA18993.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-22-1551G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32403934 | ||||||
chr9:32404040
|
T | G | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-1445T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404040 | ||||||
chr9:32404182
|
A | G | 1 | a0001c0002t0027g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-22-1303A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404182 | ||||||
chr9:32404377
|
G | C | 2 | a0001c0001t0002g0322a0001c0001t0015g0321 | 2 | HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-22-1108G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404377 | ||||||
chr9:32404670
|
T | C | 1 | a0001c0001t0019g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-22-815T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404670 | ||||||
chr9:32404671
|
C | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-22-814C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404671 | ||||||
chr9:32404685
|
G | A | 1 | a0001c0002t0002g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22-800G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404685 | ||||||
chr9:32404835
|
A | C | 1 | a0001c0006t0018g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-22-650A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404835 | ||||||
chr9:32404946
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(98): Show | 110 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22-539A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32404946 | ||||||
chr9:32405106
|
T | TAAGACTA others(5): Show |
14 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0002t0013g0064others(11): Show | 16 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-22-379_-22-378ins others(12): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405106 | ||||||
chr9:32405111
|
C | A | 14 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0002t0013g0064others(11): Show | 16 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-22-374C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405111 | ||||||
chr9:32405111
|
C | CTAGGTGG others(5): Show |
290 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(287): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-22-374_-22-373ins others(12): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405111 | ||||||
chr9:32405115
|
G | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0041others(70): Show | 78 | HG00099.hp1 HG00597.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-22-370G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405115 | ||||||
chr9:32405180
|
A | T | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0006t0003g0219others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-305A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405180 | ||||||
chr9:32405182
|
C | T | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-303C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405182 | ||||||
chr9:32405204
|
C | T | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-22-281C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405204 | ||||||
chr9:32405205
|
G | A | 2 | a0001c0002t0004g0241a0001c0002t0004g0272 | 2 | NA18969.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-22-280G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405205 | ||||||
chr9:32405213
|
C | A | 37 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(34): Show | 40 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-22-272C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405213 | ||||||
chr9:32405341
|
T | C | 1 | a0001c0002t0004g0013 | 2 | HG02015.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-22-144T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 1/20 | chr9 | 32405341 | ||||||
chr9:32405641
|
T | G | 36 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(33): Show | 39 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.97+38T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32405641 | ||||||
chr9:32405650
|
A | G | 1 | a0001c0002t0008g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97+47A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32405650 | ||||||
chr9:32405747
|
G | A | 1 | a0001c0002t0108g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97+144G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32405747 | ||||||
chr9:32405792
|
T | C | 5 | a0001c0001t0004g0310a0001c0001t0007g0030a0001c0001t0007g0311others(2): Show | 6 | HG00733.hp1 HG01175.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+189T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32405792 | ||||||
chr9:32406123
|
ATTG | A | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+523_97+525delGT others(1): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr9 | 32406123 | |||||
chr9:32406209
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(98): Show | 110 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.97+606A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406209 | ||||||
chr9:32406268
|
A | T | 113 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(110): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.97+665A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406268 | ||||||
chr9:32406312
|
A | AAT | 305 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(302): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97+712_97+713dupAT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr9 | 32406312 | |||||
chr9:32406418
|
T | G | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+815T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406418 | ||||||
chr9:32406475
|
T | A | 1 | a0001c0002t0013g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.98-786T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406475 | ||||||
chr9:32406669
|
G | A | 3 | a0001c0002t0008g0270a0001c0002t0008g0283a0005c0012t0008g0027 | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-592G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406669 | ||||||
chr9:32406823
|
G | A | 6 | a0001c0001t0001g0067a0001c0001t0003g0065a0001c0006t0003g0219others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-438G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406823 | ||||||
chr9:32406928
|
C | A | 2 | a0001c0002t0002g0104a0001c0002t0050g0103 | 2 | NA19060.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.98-333C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32406928 | ||||||
chr9:32407017
|
C | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0199 | 2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.98-244C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32407017 | ||||||
chr9:32407018
|
A | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(343): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.98-243A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32407018 | ||||||
chr9:32407208
|
C | G | 2 | a0001c0001t0014g0207a0004c0009t0024g0198 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.98-53C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 2/20 | chr9 | 32407208 | ||||||
chr9:32407468
|
A | G | 1 | a0001c0001t0006g0012 | 2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.266+39A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32407468 | ||||||
chr9:32407516
|
A | C | 9 | a0001c0001t0111g0139a0001c0001t0113g0062a0001c0011t0109g0140others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.266+87A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32407516 | ||||||
chr9:32407649
|
G | A | 1 | a0001c0002t0004g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.266+220G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32407649 | ||||||
chr9:32407684
|
C | G | 1 | a0001c0002t0010g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.266+255C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32407684 | ||||||
chr9:32407763
|
C | T | 1 | a0001c0001t0003g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.266+334C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32407763 | ||||||
chr9:32407993
|
A | G | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.267-521A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32407993 | ||||||
chr9:32408049
|
G | A | 8 | a0001c0001t0001g0072a0001c0001t0003g0074a0001c0001t0003g0075others(5): Show | 8 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.267-465G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32408049 | ||||||
chr9:32408301
|
A | G | 3 | a0001c0001t0001g0101a0001c0002t0002g0100a0001c0002t0002g0102 | 3 | NA18970.hp2 NA18993.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.267-213A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32408301 | ||||||
chr9:32408360
|
C | T | 1 | a0001c0002t0008g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.267-154C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32408360 | ||||||
chr9:32408376
|
C | G | 1 | a0001c0002t0002g0104 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.267-138C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32408376 | ||||||
chr9:32408498
|
C | G | 31 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0080others(28): Show | 33 | HG00733.hp1 HG01074.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.267-16C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 3/20 | chr9 | 32408498 | ||||||
chr9:32408814
|
G | A | 1 | a0001c0001t0090g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.404+163G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32408814 | ||||||
chr9:32409042
|
T | A | 2 | a0001c0002t0004g0227a0001c0002t0004g0242 | 2 | HG00099.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.404+391T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409042 | ||||||
chr9:32409048
|
G | A | 35 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(32): Show | 38 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.404+397G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409048 | ||||||
chr9:32409065
|
G | A | 7 | a0001c0001t0003g0065a0001c0001t0003g0074a0001c0001t0069g0059others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+414G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409065 | ||||||
chr9:32409213
|
G | A | 1 | a0009c0024t0041g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.404+562G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409213 | ||||||
chr9:32409274
|
G | A | 2 | a0001c0002t0002g0273a0001c0002t0010g0243 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.404+623G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409274 | ||||||
chr9:32409444
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(317): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.404+793G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409444 | ||||||
chr9:32409447
|
A | G | 5 | a0001c0001t0001g0265a0001c0001t0001g0282a0001c0001t0005g0239others(2): Show | 5 | HG02735.hp2 HG03017.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+796A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409447 | ||||||
chr9:32409473
|
A | G | 98 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(95): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.404+822A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409473 | ||||||
chr9:32409480
|
G | A | 1 | a0001c0025t0028g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.404+829G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409480 | ||||||
chr9:32409573
|
A | C | 206 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(203): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.404+922A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409573 | ||||||
chr9:32409731
|
G | A | 97 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(94): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.404+1080G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409731 | ||||||
chr9:32409731
|
G | C | 1 | a0001c0002t0047g0262 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.404+1080G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409731 | ||||||
chr9:32409770
|
C | A | 6 | a0001c0001t0003g0065a0001c0001t0069g0059a0001c0006t0003g0219others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.404+1119C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409770 | ||||||
chr9:32409855
|
T | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(319): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.404+1204T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32409855 | ||||||
chr9:32410310
|
G | A | 4 | a0001c0002t0027g0303a0001c0002t0027g0305a0001c0002t0027g0309others(1): Show | 5 | HG01175.hp2 HG02257.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+1659G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410310 | ||||||
chr9:32410334
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0080g0323 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.404+1683G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410334 | ||||||
chr9:32410369
|
A | T | 2 | a0001c0001t0100g0281a0001c0002t0060g0261 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.404+1718A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410369 | ||||||
chr9:32410559
|
CA | C | 39 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(36): Show | 42 | HG00280.hp1 HG01167.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.404+1918delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32410559 | |||||
chr9:32410620
|
C | A | 2 | a0003c0003t0017g0163a0003c0003t0017g0185 | 2 | NA18942.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.404+1969C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410620 | ||||||
chr9:32410749
|
T | TA | 101 | a0001c0001t0001g0238a0001c0001t0001g0265a0001c0001t0001g0278others(98): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.404+2106dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32410749 | |||||
chr9:32410795
|
G | A | 1 | a0001c0001t0097g0046 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.404+2144G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410795 | ||||||
chr9:32410852
|
T | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(320): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.404+2201T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410852 | ||||||
chr9:32410872
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(96): Show | 108 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.404+2221A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32410872 | ||||||
chr9:32411048
|
A | G | 1 | a0001c0002t0038g0328 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.404+2397A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411048 | ||||||
chr9:32411154
|
G | A | 1 | a0001c0002t0002g0107 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.404+2503G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411154 | ||||||
chr9:32411195
|
C | A | 1 | a0001c0005t0081g0314 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404+2544C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411195 | ||||||
chr9:32411237
|
G | A | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+2586G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411237 | ||||||
chr9:32411495
|
T | C | 3 | a0001c0006t0018g0032a0001c0006t0018g0330a0001c0006t0105g0315 | 4 | HG02280.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+2844T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411495 | ||||||
chr9:32411591
|
T | G | 1 | a0001c0001t0102g0295 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.404+2940T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411591 | ||||||
chr9:32411614
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.404+2963A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411614 | ||||||
chr9:32411961
|
C | T | 3 | a0001c0002t0038g0301a0001c0011t0109g0140a0001c0011t0110g0141 | 3 | HG02486.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.404+3310C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32411961 | ||||||
chr9:32412293
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(60): Show | 69 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.404+3642C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412293 | ||||||
chr9:32412342
|
T | C | 2 | a0001c0001t0040g0212a0001c0001t0040g0213 | 2 | NA19000.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.404+3691T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412342 | ||||||
chr9:32412541
|
A | G | 1 | a0001c0001t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.404+3890A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412541 | ||||||
chr9:32412624
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(60): Show | 69 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.404+3973C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412624 | ||||||
chr9:32412774
|
G | T | 1 | a0001c0002t0068g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.404+4123G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412774 | ||||||
chr9:32412823
|
A | G | 1 | a0001c0001t0069g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.404+4172A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412823 | ||||||
chr9:32412870
|
T | A | 3 | a0001c0001t0029g0017a0001c0001t0077g0017a0001c0002t0002g0144 | 3 | HG00639.hp1 HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.404+4219T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412870 | ||||||
chr9:32412981
|
G | T | 1 | a0001c0002t0012g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.404+4330G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32412981 | ||||||
chr9:32413026
|
A | AT | 6 | a0001c0001t0007g0311a0001c0001t0085g0206a0001c0001t0111g0139others(3): Show | 6 | HG01515.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.404+4387dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32413026 | |||||
chr9:32413100
|
G | A | 2 | a0001c0001t0040g0212a0001c0001t0040g0213 | 2 | NA19000.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.404+4449G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32413100 | ||||||
chr9:32413278
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.404+4627G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32413278 | ||||||
chr9:32413303
|
G | A | 1 | a0012c0028t0007g0266 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.404+4652G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32413303 | ||||||
chr9:32413326
|
T | C | 1 | a0001c0002t0008g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.404+4675T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32413326 | ||||||
chr9:32413341
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.404+4690G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32413341 | ||||||
chr9:32413398
|
C | T | 1 | a0001c0008t0032g0326 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.405-4730C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32413398 | ||||||
chr9:32413482
|
C | CA | 6 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0003g0075others(3): Show | 6 | HG01074.hp1 HG01361.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-4626dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32413482 | |||||
chr9:32413482
|
CA | C | 17 | a0001c0001t0007g0271a0001c0001t0040g0212a0001c0001t0080g0323others(14): Show | 18 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.405-4626delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32413482 | |||||
chr9:32413482
|
CAA | C | 160 | a0001c0001t0001g0053a0001c0001t0001g0151a0001c0001t0001g0176others(157): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.405-4627_405-4626d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32413482 | |||||
chr9:32413482
|
CAAA | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(96): Show | 108 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.405-4628_405-4626d others(5): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32413482 | |||||
chr9:32414061
|
G | A | 34 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(31): Show | 37 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.405-4067G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32414061 | ||||||
chr9:32414084
|
C | A | 1 | a0001c0002t0001g0167 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.405-4044C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32414084 | ||||||
chr9:32414093
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.405-4035C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32414093 | ||||||
chr9:32414101
|
C | T | 34 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(31): Show | 37 | HG00099.hp1 HG00597.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.405-4027C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32414101 | ||||||
chr9:32414162
|
G | A | 44 | a0001c0001t0001g0101a0001c0001t0001g0108a0001c0001t0001g0110others(41): Show | 47 | HG00280.hp1 HG01175.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.405-3966G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32414162 | ||||||
chr9:32414600
|
T | TG | 6 | a0001c0001t0002g0149a0001c0001t0029g0017a0001c0001t0029g0148others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-3524dupG | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32414600 | |||||
chr9:32414856
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.405-3272C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32414856 | ||||||
chr9:32415001
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0003g0177 | 2 | NA18959.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.405-3127G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415001 | ||||||
chr9:32415035
|
G | C | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-3093G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415035 | ||||||
chr9:32415130
|
G | A | 2 | a0001c0002t0038g0301a0001c0002t0083g0300 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.405-2998G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415130 | ||||||
chr9:32415301
|
T | C | 1 | a0001c0001t0007g0271 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.405-2827T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415301 | ||||||
chr9:32415639
|
T | A | 1 | a0001c0002t0010g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-2489T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415639 | ||||||
chr9:32415673
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.405-2455C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415673 | ||||||
chr9:32415919
|
T | C | 2 | a0001c0001t0001g0151a0001c0002t0010g0150 | 2 | HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.405-2209T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32415919 | ||||||
chr9:32416097
|
C | CT | 164 | a0001c0001t0001g0151a0001c0001t0001g0176a0001c0001t0001g0238others(161): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.405-2016dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr9 | 32416097 | |||||
chr9:32416121
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0329 | 3 | NA18947.hp1 NA18982.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.405-2007G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416121 | ||||||
chr9:32416127
|
C | A | 1 | a0001c0001t0106g0038 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.405-2001C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416127 | ||||||
chr9:32416133
|
C | T | 62 | a0001c0001t0001g0151a0001c0001t0001g0176a0001c0001t0002g0149others(59): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.405-1995C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416133 | ||||||
chr9:32416156
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(61): Show | 70 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.405-1972G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416156 | ||||||
chr9:32416157
|
C | A | 2 | a0002c0004t0023g0008a0002c0004t0064g0223 | 4 | HG01070.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-1971C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416157 | ||||||
chr9:32416219
|
C | T | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.405-1909C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416219 | ||||||
chr9:32416255
|
C | T | 1 | a0001c0001t0010g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.405-1873C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416255 | ||||||
chr9:32416329
|
G | A | 1 | a0001c0001t0087g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.405-1799G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416329 | ||||||
chr9:32416388
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(96): Show | 108 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.405-1740C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416388 | ||||||
chr9:32416431
|
C | T | 1 | a0001c0001t0111g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.405-1697C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416431 | ||||||
chr9:32416483
|
C | T | 84 | a0001c0001t0001g0265a0001c0001t0001g0278a0001c0001t0001g0282others(81): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.405-1645C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416483 | ||||||
chr9:32416524
|
A | G | 5 | a0001c0001t0003g0065a0001c0006t0003g0219a0001c0006t0018g0217others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-1604A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416524 | ||||||
chr9:32416936
|
G | A | 6 | a0001c0001t0003g0065a0001c0002t0027g0303a0001c0002t0027g0305others(3): Show | 7 | HG01175.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-1192G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32416936 | ||||||
chr9:32417033
|
G | A | 1 | a0001c0002t0065g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.405-1095G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417033 | ||||||
chr9:32417221
|
T | C | 2 | a0001c0011t0109g0140a0001c0011t0110g0141 | 2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.405-907T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417221 | ||||||
chr9:32417246
|
C | T | 230 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(227): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.405-882C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417246 | ||||||
chr9:32417393
|
C | T | 1 | a0001c0002t0004g0325 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.405-735C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417393 | ||||||
chr9:32417619
|
A | G | 1 | a0001c0002t0009g0259 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.405-509A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417619 | ||||||
chr9:32417623
|
T | G | 133 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0002t0001g0019others(130): Show | 148 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.405-505T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417623 | ||||||
chr9:32417731
|
C | A | 6 | a0001c0002t0027g0303a0001c0002t0027g0305a0001c0002t0027g0309others(3): Show | 7 | HG01175.hp2 HG01243.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-397C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417731 | ||||||
chr9:32417731
|
C | T | 1 | a0001c0001t0102g0295 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.405-397C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417731 | ||||||
chr9:32417893
|
C | T | 12 | a0001c0001t0001g0151a0001c0001t0002g0149a0001c0001t0006g0152others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.405-235C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 4/20 | chr9 | 32417893 | ||||||
chr9:32418239
|
G | T | 227 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(224): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.474+42G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 5/20 | chr9 | 32418239 | ||||||
chr9:32418279
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0080a0001c0001t0003g0078others(7): Show | 11 | HG02015.hp2 HG02080.hp2 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-49T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 5/20 | chr9 | 32418279 | ||||||
chr9:32418294
|
C | T | 2 | a0001c0002t0038g0301a0001c0002t0083g0300 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.475-34C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 5/20 | chr9 | 32418294 | ||||||
chr9:32418689
|
A | G | 1 | a0002c0004t0014g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.658+178A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 6/20 | chr9 | 32418689 | ||||||
chr9:32419251
|
G | A | 3 | a0001c0001t0111g0139a0001c0002t0038g0328a0001c0019t0112g0138 | 3 | HG02572.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.798+74G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419251 | ||||||
chr9:32419463
|
C | T | 52 | a0001c0001t0001g0101a0001c0001t0001g0151a0001c0001t0001g0176others(49): Show | 54 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.798+286C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419463 | ||||||
chr9:32419602
|
A | G | 6 | a0002c0007t0031g0094a0002c0007t0031g0316a0002c0007t0042g0096others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+425A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419602 | ||||||
chr9:32419830
|
T | C | 8 | a0001c0001t0003g0065a0001c0001t0069g0059a0001c0002t0038g0301others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+653T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419830 | ||||||
chr9:32419914
|
A | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.798+737A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419914 | ||||||
chr9:32419942
|
A | T | 1 | a0001c0002t0002g0125 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.798+765A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419942 | ||||||
chr9:32419952
|
G | A | 1 | a0001c0002t0002g0244 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.798+775G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32419952 | ||||||
chr9:32420100
|
T | TTCCATAT others(62): Show |
37 | a0001c0001t0001g0053a0001c0001t0003g0005a0001c0001t0003g0051others(34): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.799-753_799-685dup others(69): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr9 | 32420100 | |||||
chr9:32420191
|
C | T | 3 | a0001c0001t0111g0139a0001c0002t0038g0328a0001c0019t0112g0138 | 3 | HG02572.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.799-665C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32420191 | ||||||
chr9:32420349
|
G | A | 2 | a0001c0002t0038g0301a0001c0002t0083g0300 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.799-507G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32420349 | ||||||
chr9:32420351
|
T | G | 128 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0002t0001g0019others(125): Show | 142 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.799-505T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32420351 | ||||||
chr9:32420368
|
G | C | 1 | a0001c0001t0004g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.799-488G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32420368 | ||||||
chr9:32420639
|
A | G | 3 | a0002c0004t0023g0008a0002c0004t0023g0158a0002c0004t0064g0223 | 5 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-217A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32420639 | ||||||
chr9:32420814
|
G | A | 2 | a0001c0002t0026g0245a0001c0002t0026g0274 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.799-42G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 7/20 | chr9 | 32420814 | ||||||
chr9:32421639
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0005g0306others(2): Show | 5 | HG02886.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+612A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32421639 | ||||||
chr9:32421664
|
C | T | 3 | a0001c0001t0111g0139a0001c0002t0038g0328a0001c0019t0112g0138 | 3 | HG02572.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.970+637C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32421664 | ||||||
chr9:32421806
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.970+779G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32421806 | ||||||
chr9:32421984
|
G | A | 245 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(242): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.970+957G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32421984 | ||||||
chr9:32422090
|
G | A | 3 | a0001c0002t0002g0178a0001c0002t0002g0181a0001c0002t0067g0170 | 3 | NA18953.hp1 NA18956.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.970+1063G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422090 | ||||||
chr9:32422404
|
A | T | 87 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(84): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.971-915A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422404 | ||||||
chr9:32422561
|
G | A | 3 | a0002c0004t0023g0008a0002c0004t0023g0158a0002c0004t0064g0223 | 5 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-758G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422561 | ||||||
chr9:32422658
|
G | C | 5 | a0001c0002t0008g0235a0001c0002t0008g0236a0001c0002t0008g0237others(2): Show | 5 | HG01496.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.971-661G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422658 | ||||||
chr9:32422692
|
T | A | 245 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(242): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.971-627T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422692 | ||||||
chr9:32422811
|
A | G | 3 | a0001c0001t0014g0207a0001c0001t0014g0226a0004c0009t0024g0198 | 3 | HG02109.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.971-508A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422811 | ||||||
chr9:32422928
|
C | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.971-391C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422928 | ||||||
chr9:32422937
|
T | C | 1 | a0004c0027t0024g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.971-382T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32422937 | ||||||
chr9:32423013
|
T | C | 1 | a0001c0001t0069g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.971-306T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423013 | ||||||
chr9:32423046
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0005g0006a0001c0001t0005g0082others(3): Show | 7 | NA18942.hp2 NA18946.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.971-273C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423046 | ||||||
chr9:32423079
|
C | G | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.971-240C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423079 | ||||||
chr9:32423174
|
C | T | 7 | a0001c0001t0003g0007a0001c0001t0003g0018a0001c0001t0003g0159others(4): Show | 8 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.971-145C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423174 | ||||||
chr9:32423195
|
G | C | 1 | a0001c0002t0012g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.971-124G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423195 | ||||||
chr9:32423276
|
A | T | 6 | a0002c0007t0031g0094a0002c0007t0031g0316a0002c0007t0042g0096others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.971-43A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423276 | ||||||
chr9:32423302
|
C | T | 6 | a0002c0007t0031g0094a0002c0007t0031g0316a0002c0007t0042g0096others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.971-17C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 8/20 | chr9 | 32423302 | ||||||
chr9:32423502
|
G | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1071+83G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423502 | ||||||
chr9:32423567
|
C | G | 8 | a0001c0002t0027g0303a0001c0002t0027g0305a0001c0002t0027g0309others(5): Show | 9 | HG01175.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+148C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423567 | ||||||
chr9:32423578
|
G | A | 1 | a0004c0027t0024g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1071+159G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423578 | ||||||
chr9:32423580
|
C | A | 1 | a0004c0027t0024g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1071+161C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423580 | ||||||
chr9:32423606
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1071+187A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423606 | ||||||
chr9:32423694
|
A | G | 14 | a0001c0001t0003g0065a0001c0001t0069g0059a0001c0002t0027g0303others(11): Show | 15 | HG01175.hp2 HG01243.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+275A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423694 | ||||||
chr9:32423754
|
C | A | 3 | a0001c0006t0018g0032a0001c0006t0018g0330a0001c0006t0105g0315 | 4 | HG02280.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+335C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423754 | ||||||
chr9:32423815
|
C | T | 1 | a0001c0002t0038g0328 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1071+396C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423815 | ||||||
chr9:32423849
|
C | G | 125 | a0001c0001t0001g0238a0001c0001t0001g0278a0001c0002t0001g0019others(122): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1071+430C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32423849 | ||||||
chr9:32424083
|
T | C | 1 | a0001c0008t0032g0086 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1072-466T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424083 | ||||||
chr9:32424085
|
G | A | 1 | a0001c0001t0007g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1072-464G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424085 | ||||||
chr9:32424212
|
C | T | 88 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(85): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1072-337C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424212 | ||||||
chr9:32424227
|
A | G | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1072-322A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424227 | ||||||
chr9:32424261
|
C | T | 1 | a0003c0003t0017g0185 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1072-288C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424261 | ||||||
chr9:32424263
|
A | G | 1 | a0001c0002t0004g0049 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1072-286A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424263 | ||||||
chr9:32424288
|
C | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1072-261C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424288 | ||||||
chr9:32424355
|
G | C | 226 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(223): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1072-194G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424355 | ||||||
chr9:32424364
|
G | A | 87 | a0001c0001t0001g0278a0001c0002t0001g0019a0001c0002t0001g0026others(84): Show | 98 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1072-185G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 9/20 | chr9 | 32424364 | ||||||
chr9:32424700
|
A | G | 12 | a0001c0001t0111g0139a0001c0002t0038g0328a0001c0011t0109g0140others(9): Show | 14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1188+35A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32424700 | ||||||
chr9:32424726
|
C | T | 7 | a0001c0019t0112g0138a0002c0004t0001g0135a0002c0004t0001g0137others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1188+61C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32424726 | ||||||
chr9:32424839
|
G | A | 6 | a0001c0002t0002g0171a0001c0005t0013g0029a0001c0005t0013g0304others(3): Show | 7 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1188+174G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32424839 | ||||||
chr9:32424895
|
A | G | 191 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(188): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1188+230A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32424895 | ||||||
chr9:32424902
|
C | G | 180 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(177): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1188+237C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32424902 | ||||||
chr9:32424912
|
C | G | 3 | a0002c0004t0023g0008a0002c0004t0023g0158a0002c0004t0064g0223 | 5 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1188+247C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32424912 | ||||||
chr9:32424916
|
T | TTACTC | 103 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(100): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1188+252_1188+256d others(7): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr9 | 32424916 | |||||
chr9:32425113
|
G | T | 6 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+448G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425113 | ||||||
chr9:32425126
|
G | A | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1188+461G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425126 | ||||||
chr9:32425127
|
A | T | 1 | a0001c0001t0004g0044 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1188+462A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425127 | ||||||
chr9:32425272
|
G | A | 136 | a0001c0001t0001g0278a0001c0002t0001g0019a0001c0002t0001g0026others(133): Show | 152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1189-566G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425272 | ||||||
chr9:32425388
|
A | G | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1189-450A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425388 | ||||||
chr9:32425403
|
T | C | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1189-435T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425403 | ||||||
chr9:32425678
|
T | G | 162 | a0001c0001t0003g0065a0001c0001t0069g0059a0001c0002t0001g0019others(159): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1189-160T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425678 | ||||||
chr9:32425810
|
A | G | 1 | a0001c0010t0028g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1189-28A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 10/20 | chr9 | 32425810 | ||||||
chr9:32426198
|
C | T | 4 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0018g0179others(1): Show | 4 | HG01069.hp2 HG01192.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+201C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426198 | ||||||
chr9:32426348
|
A | G | 1 | a0001c0019t0112g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1348+351A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426348 | ||||||
chr9:32426554
|
C | T | 1 | a0004c0027t0024g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1348+557C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426554 | ||||||
chr9:32426763
|
T | C | 1 | a0001c0002t0103g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1349-538T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426763 | ||||||
chr9:32426792
|
T | C | 1 | a0001c0001t0014g0186 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1349-509T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426792 | ||||||
chr9:32426929
|
A | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1349-372A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426929 | ||||||
chr9:32426978
|
CT | C | 3 | a0001c0011t0109g0140a0001c0011t0110g0141a0001c0025t0028g0070 | 3 | HG02486.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1349-322delT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32426978 | ||||||
chr9:32426979
|
TA | T | 236 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0151others(233): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1349-312delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr9 | 32426979 | |||||
chr9:32426979
|
TAA | T | 6 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1349-313_1349-312d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr9 | 32426979 | |||||
chr9:32427065
|
T | C | 1 | a0001c0001t0004g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1349-236T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32427065 | ||||||
chr9:32427079
|
G | A | 4 | a0001c0011t0109g0140a0001c0011t0110g0141a0001c0025t0028g0070others(1): Show | 4 | HG02486.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349-222G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32427079 | ||||||
chr9:32427101
|
T | A | 3 | a0001c0011t0109g0140a0001c0011t0110g0141a0001c0025t0028g0070 | 3 | HG02486.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1349-200T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32427101 | ||||||
chr9:32427277
|
G | A | 1 | a0001c0002t0004g0228 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1349-24G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 11/20 | chr9 | 32427277 | ||||||
chr9:32427483
|
C | T | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1484+47C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427483 | ||||||
chr9:32427537
|
A | G | 8 | a0001c0001t0113g0062a0001c0002t0008g0180a0002c0004t0001g0135others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1484+101A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427537 | ||||||
chr9:32427540
|
T | C | 1 | a0001c0001t0030g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1484+104T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427540 | ||||||
chr9:32427553
|
G | A | 1 | a0001c0001t0024g0307 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1484+117G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427553 | ||||||
chr9:32427594
|
C | G | 54 | a0001c0001t0001g0053a0001c0001t0003g0005a0001c0001t0003g0051others(51): Show | 57 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1484+158C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427594 | ||||||
chr9:32427602
|
A | G | 329 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(326): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1484+166A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427602 | ||||||
chr9:32427617
|
T | C | 1 | a0001c0001t0004g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1484+181T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427617 | ||||||
chr9:32427750
|
T | G | 7 | a0001c0002t0013g0064a0001c0002t0034g0222a0001c0002t0038g0301others(4): Show | 7 | HG01255.hp1 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1484+314T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427750 | ||||||
chr9:32427800
|
C | T | 18 | a0001c0002t0001g0019a0001c0002t0002g0003a0001c0002t0002g0107others(15): Show | 22 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1484+364C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427800 | ||||||
chr9:32427876
|
A | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(97): Show | 107 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1484+440A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427876 | ||||||
chr9:32427927
|
G | C | 1 | a0001c0001t0036g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1484+491G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32427927 | ||||||
chr9:32428068
|
A | C | 33 | a0001c0001t0004g0042a0001c0001t0004g0183a0001c0001t0006g0011others(30): Show | 35 | HG00597.hp2 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1484+632A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428068 | ||||||
chr9:32428087
|
C | A | 6 | a0001c0002t0004g0228a0001c0002t0004g0247a0001c0002t0004g0248others(3): Show | 6 | HG02074.hp1 HG02083.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1484+651C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428087 | ||||||
chr9:32428112
|
CA | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(153): Show | 168 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.1484+688delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr9 | 32428112 | |||||
chr9:32428112
|
CAA | C | 6 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1484+687_1484+688d others(4): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr9 | 32428112 | |||||
chr9:32428121
|
A | G | 3 | a0002c0004t0001g0135a0002c0004t0001g0137a0002c0004t0014g0136 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1484+685A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428121 | ||||||
chr9:32428211
|
G | A | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1484+775G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428211 | ||||||
chr9:32428219
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0208a0001c0002t0005g0128others(1): Show | 4 | HG00558.hp2 NA18949.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484+783G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428219 | ||||||
chr9:32428281
|
C | CA | 155 | a0001c0001t0001g0151a0001c0001t0001g0157a0001c0001t0001g0176others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1484+863dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr9 | 32428281 | |||||
chr9:32428281
|
CA | C | 26 | a0001c0001t0001g0331a0001c0001t0007g0271a0001c0001t0021g0193others(23): Show | 26 | HG01099.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1484+863delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr9 | 32428281 | |||||
chr9:32428414
|
G | A | 1 | a0001c0001t0022g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1484+978G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428414 | ||||||
chr9:32428444
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(280): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1485-975C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428444 | ||||||
chr9:32428478
|
G | C | 16 | a0001c0002t0013g0064a0001c0002t0027g0303a0001c0002t0027g0305others(13): Show | 17 | HG01175.hp2 HG01255.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1485-941G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428478 | ||||||
chr9:32428564
|
C | T | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1485-855C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428564 | ||||||
chr9:32428590
|
G | T | 6 | a0001c0001t0113g0062a0001c0002t0038g0301a0001c0002t0038g0328others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1485-829G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32428590 | ||||||
chr9:32428843
|
C | CA | 45 | a0001c0001t0004g0183a0001c0001t0005g0264a0001c0001t0006g0011others(42): Show | 48 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1485-564dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr9 | 32428843 | |||||
chr9:32429087
|
A | G | 3 | a0001c0002t0038g0301a0001c0002t0038g0328a0001c0002t0083g0300 | 3 | HG02572.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1485-332A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32429087 | ||||||
chr9:32429216
|
A | G | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485-203A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32429216 | ||||||
chr9:32429221
|
A | G | 7 | a0001c0001t0003g0007a0001c0001t0003g0018a0001c0001t0003g0065others(4): Show | 8 | HG02280.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1485-198A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32429221 | ||||||
chr9:32429239
|
C | A | 31 | a0001c0001t0004g0183a0001c0001t0005g0264a0001c0001t0006g0011others(28): Show | 33 | HG00597.hp2 HG00642.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1485-180C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32429239 | ||||||
chr9:32429259
|
G | A | 7 | a0001c0001t0001g0238a0001c0002t0027g0303a0001c0002t0027g0305others(4): Show | 7 | HG01175.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485-160G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 12/20 | chr9 | 32429259 | ||||||
chr9:32429523
|
C | T | 3 | a0004c0009t0024g0198a0004c0009t0051g0084a0004c0027t0024g0215 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1569+20C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 13/20 | chr9 | 32429523 | ||||||
chr9:32429577
|
T | G | 4 | a0001c0001t0033g0145a0001c0001t0033g0147a0001c0001t0076g0061others(1): Show | 4 | HG00741.hp2 HG01106.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+74T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 13/20 | chr9 | 32429577 | ||||||
chr9:32429605
|
T | C | 4 | a0001c0002t0008g0235a0001c0002t0008g0236a0001c0002t0008g0285others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+102T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 13/20 | chr9 | 32429605 | ||||||
chr9:32429622
|
T | C | 20 | a0001c0001t0001g0238a0001c0001t0113g0062a0001c0002t0027g0303others(17): Show | 20 | HG01175.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1569+119T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 13/20 | chr9 | 32429622 | ||||||
chr9:32429622
|
T | G | 1 | a0001c0019t0112g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1569+119T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 13/20 | chr9 | 32429622 | ||||||
chr9:32429976
|
C | T | 3 | a0004c0009t0024g0198a0004c0009t0051g0084a0004c0027t0024g0215 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1570-442C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 13/20 | chr9 | 32429976 | ||||||
chr9:32430639
|
C | T | 1 | a0001c0001t0069g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1726+65C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32430639 | ||||||
chr9:32430680
|
A | G | 23 | a0001c0001t0001g0238a0001c0001t0069g0059a0001c0001t0113g0062others(20): Show | 23 | HG01175.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1726+106A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32430680 | ||||||
chr9:32430916
|
A | G | 1 | a0001c0019t0112g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1726+342A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32430916 | ||||||
chr9:32431004
|
A | G | 3 | a0001c0001t0053g0313a0001c0001t0054g0312a0001c0002t0005g0253 | 3 | HG01175.hp1 HG02145.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1726+430A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431004 | ||||||
chr9:32431078
|
C | T | 1 | a0001c0001t0015g0231 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1726+504C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431078 | ||||||
chr9:32431111
|
G | A | 1 | a0001c0002t0002g0104 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1726+537G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431111 | ||||||
chr9:32431171
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1727-548C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431171 | ||||||
chr9:32431273
|
T | C | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1727-446T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431273 | ||||||
chr9:32431275
|
C | T | 4 | a0001c0002t0038g0301a0001c0002t0038g0328a0001c0002t0083g0300others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727-444C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431275 | ||||||
chr9:32431308
|
G | A | 46 | a0001c0001t0004g0183a0001c0001t0005g0264a0001c0001t0006g0011others(43): Show | 49 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.1727-411G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431308 | ||||||
chr9:32431595
|
A | G | 3 | a0004c0009t0024g0198a0004c0009t0051g0084a0004c0027t0024g0215 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1727-124A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431595 | ||||||
chr9:32431622
|
T | C | 8 | a0001c0001t0001g0238a0001c0001t0069g0059a0001c0002t0027g0303others(5): Show | 8 | HG01175.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1727-97T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431622 | ||||||
chr9:32431678
|
A | G | 1 | a0001c0019t0112g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1727-41A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 14/20 | chr9 | 32431678 | ||||||
chr9:32431893
|
G | C | 2 | a0001c0008t0032g0086a0001c0008t0032g0326 | 2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1851+50G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32431893 | ||||||
chr9:32431933
|
A | G | 128 | a0001c0001t0001g0238a0001c0001t0002g0149a0001c0001t0002g0168others(125): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1851+90A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32431933 | ||||||
chr9:32431939
|
A | G | 1 | a0001c0001t0003g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1851+96A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32431939 | ||||||
chr9:32432028
|
C | T | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+185C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432028 | ||||||
chr9:32432135
|
A | G | 41 | a0001c0001t0002g0149a0001c0001t0002g0322a0001c0001t0010g0187others(38): Show | 45 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1851+292A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432135 | ||||||
chr9:32432157
|
G | A | 1 | a0001c0002t0013g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1851+314G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432157 | ||||||
chr9:32432197
|
G | T | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+354G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432197 | ||||||
chr9:32432303
|
G | A | 5 | a0001c0001t0053g0313a0001c0001t0054g0312a0001c0002t0005g0253others(2): Show | 5 | HG01175.hp1 HG01256.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851+460G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432303 | ||||||
chr9:32432365
|
A | T | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1851+522A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432365 | ||||||
chr9:32432405
|
G | C | 1 | a0001c0002t0013g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1851+562G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432405 | ||||||
chr9:32432443
|
A | G | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1851+600A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432443 | ||||||
chr9:32432567
|
C | T | 110 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(107): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1851+724C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432567 | ||||||
chr9:32432649
|
T | C | 127 | a0001c0001t0001g0238a0001c0001t0002g0149a0001c0001t0002g0168others(124): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1851+806T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432649 | ||||||
chr9:32432650
|
G | A | 1 | a0001c0002t0002g0142 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1851+807G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432650 | ||||||
chr9:32432683
|
T | G | 128 | a0001c0001t0001g0238a0001c0001t0002g0149a0001c0001t0002g0168others(125): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1851+840T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432683 | ||||||
chr9:32432976
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(180): Show | 199 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.1852-752G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32432976 | ||||||
chr9:32433359
|
G | A | 3 | a0004c0009t0024g0198a0004c0009t0051g0084a0004c0027t0024g0215 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1852-369G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32433359 | ||||||
chr9:32433499
|
G | A | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-229G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32433499 | ||||||
chr9:32433505
|
G | A | 1 | a0001c0002t0001g0026 | 2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1852-223G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32433505 | ||||||
chr9:32433512
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0204 | 2 | NA19001.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1852-216T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32433512 | ||||||
chr9:32433528
|
T | C | 120 | a0001c0001t0001g0238a0001c0001t0002g0168a0001c0001t0004g0042others(117): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.1852-200T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 15/20 | chr9 | 32433528 | ||||||
chr9:32433963
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(186): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1956+131C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32433963 | ||||||
chr9:32433964
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0005g0021 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1956+132T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32433964 | ||||||
chr9:32433967
|
T | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(316): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1956+135T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32433967 | ||||||
chr9:32433984
|
G | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0004g0090others(4): Show | 7 | HG02886.hp2 HG03225.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+152G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32433984 | ||||||
chr9:32434010
|
C | G | 1 | a0001c0002t0002g0100 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1956+178C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434010 | ||||||
chr9:32434060
|
G | T | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+228G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434060 | ||||||
chr9:32434063
|
A | G | 2 | a0001c0011t0109g0140a0001c0011t0110g0141 | 2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1956+231A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434063 | ||||||
chr9:32434168
|
C | T | 1 | a0006c0014t0012g0251 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1956+336C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434168 | ||||||
chr9:32434178
|
A | G | 6 | a0001c0001t0022g0002a0001c0001t0022g0033a0001c0001t0099g0083others(3): Show | 7 | NA18953.hp2 NA18960.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+346A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434178 | ||||||
chr9:32434318
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1957-241T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434318 | ||||||
chr9:32434393
|
T | G | 1 | a0001c0006t0003g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1957-166T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 16/20 | chr9 | 32434393 | ||||||
chr9:32434726
|
A | T | 1 | a0006c0014t0012g0251 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2099+25A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32434726 | ||||||
chr9:32434844
|
T | C | 2 | a0001c0011t0109g0140a0001c0011t0110g0141 | 2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2099+143T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32434844 | ||||||
chr9:32434997
|
G | A | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2099+296G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32434997 | ||||||
chr9:32435046
|
T | C | 4 | a0001c0001t0080g0323a0001c0002t0038g0301a0001c0002t0038g0328others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099+345T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435046 | ||||||
chr9:32435135
|
G | A | 2 | a0002c0007t0031g0094a0002c0007t0031g0316 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2099+434G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435135 | ||||||
chr9:32435173
|
A | G | 1 | a0001c0002t0013g0064 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2099+472A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435173 | ||||||
chr9:32435179
|
T | C | 3 | a0001c0001t0015g0035a0001c0001t0100g0281a0001c0001t0102g0295 | 3 | HG00323.hp1 HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2099+478T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435179 | ||||||
chr9:32435289
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2099+588T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435289 | ||||||
chr9:32435340
|
T | G | 4 | a0001c0001t0007g0205a0001c0001t0007g0271a0001c0001t0084g0267others(1): Show | 4 | HG01099.hp1 HG01358.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099+639T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435340 | ||||||
chr9:32435370
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2099+669C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435370 | ||||||
chr9:32435519
|
A | G | 7 | a0001c0001t0001g0238a0001c0002t0027g0303a0001c0002t0027g0305others(4): Show | 7 | HG01175.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2100-731A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435519 | ||||||
chr9:32435678
|
A | G | 117 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(114): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2100-572A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435678 | ||||||
chr9:32435703
|
G | A | 8 | a0001c0011t0109g0140a0001c0011t0110g0141a0001c0019t0112g0138others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2100-547G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435703 | ||||||
chr9:32435980
|
C | T | 119 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(116): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2100-270C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32435980 | ||||||
chr9:32436016
|
A | G | 190 | a0001c0001t0001g0238a0001c0001t0002g0149a0001c0001t0002g0168others(187): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2100-234A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32436016 | ||||||
chr9:32436109
|
T | G | 3 | a0001c0001t0004g0044a0001c0001t0004g0199a0001c0001t0004g0310 | 3 | HG00099.hp1 HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2100-141T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32436109 | ||||||
chr9:32436226
|
C | T | 1 | a0001c0002t0002g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2100-24C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 17/20 | chr9 | 32436226 | ||||||
chr9:32436682
|
C | T | 7 | a0001c0001t0001g0238a0001c0002t0027g0303a0001c0002t0027g0305others(4): Show | 7 | HG01175.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2247+285C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32436682 | ||||||
chr9:32436685
|
G | C | 114 | a0001c0001t0002g0168a0001c0001t0004g0042a0001c0001t0004g0044others(111): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.2247+288G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32436685 | ||||||
chr9:32436905
|
A | G | 32 | a0001c0001t0004g0183a0001c0001t0005g0264a0001c0001t0006g0011others(29): Show | 34 | HG00597.hp2 HG00642.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2247+508A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32436905 | ||||||
chr9:32436956
|
C | T | 4 | a0001c0001t0080g0323a0001c0002t0038g0301a0001c0002t0038g0328others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247+559C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32436956 | ||||||
chr9:32436996
|
C | G | 2 | a0001c0002t0006g0263a0001c0002t0107g0232 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2247+599C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32436996 | ||||||
chr9:32437136
|
G | A | 1 | a0001c0001t0080g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2247+739G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32437136 | ||||||
chr9:32437244
|
C | G | 1 | a0001c0001t0019g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2247+847C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32437244 | ||||||
chr9:32437251
|
T | C | 126 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(123): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.2247+854T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32437251 | ||||||
chr9:32437419
|
A | AATAATCA others(3): Show |
23 | a0001c0001t0001g0238a0001c0001t0069g0059a0001c0002t0027g0303others(20): Show | 23 | HG01175.hp2 HG01192.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2247+1026_2247+102 others(14): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr9 | 32437419 | |||||
chr9:32437444
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0282a0001c0001t0005g0239 | 3 | HG02735.hp2 HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2247+1047C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32437444 | ||||||
chr9:32437614
|
G | C | 1 | a0001c0001t0021g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2247+1217G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32437614 | ||||||
chr9:32437738
|
A | C | 23 | a0001c0001t0001g0238a0001c0001t0069g0059a0001c0002t0027g0303others(20): Show | 23 | HG01175.hp2 HG01192.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2247+1341A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32437738 | ||||||
chr9:32438477
|
C | A | 1 | a0001c0001t0019g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2248-1988C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32438477 | ||||||
chr9:32438692
|
A | T | 36 | a0001c0001t0010g0187a0001c0001t0010g0195a0001c0002t0002g0003others(33): Show | 40 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2248-1773A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32438692 | ||||||
chr9:32438877
|
T | G | 1 | a0001c0001t0006g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2248-1588T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32438877 | ||||||
chr9:32439129
|
G | A | 1 | a0001c0001t0020g0327 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2248-1336G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32439129 | ||||||
chr9:32439346
|
T | C | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2248-1119T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32439346 | ||||||
chr9:32439407
|
A | T | 1 | a0001c0001t0005g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2248-1058A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32439407 | ||||||
chr9:32439524
|
A | G | 1 | a0001c0002t0008g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2248-941A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32439524 | ||||||
chr9:32439613
|
C | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2248-852C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32439613 | ||||||
chr9:32439797
|
C | T | 19 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(16): Show | 21 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.2248-668C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32439797 | ||||||
chr9:32440033
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2248-432G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32440033 | ||||||
chr9:32440140
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2248-325G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32440140 | ||||||
chr9:32440267
|
C | CA | 8 | a0001c0002t0005g0128a0001c0025t0028g0070a0002c0004t0023g0008others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2248-184dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr9 | 32440267 | |||||
chr9:32440385
|
C | T | 4 | a0001c0001t0080g0323a0004c0009t0024g0198a0004c0009t0051g0084others(1): Show | 4 | HG02886.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248-80C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32440385 | ||||||
chr9:32440406
|
G | C | 49 | a0001c0001t0004g0183a0001c0001t0005g0264a0001c0001t0006g0011others(46): Show | 52 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.2248-59G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 18/20 | chr9 | 32440406 | ||||||
chr9:32440615
|
G | T | 2 | a0001c0001t0005g0306a0001c0001t0024g0307 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2370+28G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32440615 | ||||||
chr9:32440637
|
G | T | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2370+50G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32440637 | ||||||
chr9:32440667
|
C | T | 1 | a0001c0002t0093g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2370+80C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32440667 | ||||||
chr9:32440793
|
A | G | 4 | a0002c0007t0031g0094a0002c0007t0031g0316a0002c0007t0042g0096others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2370+206A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32440793 | ||||||
chr9:32441155
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(67): Show | 77 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.2370+568G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441155 | ||||||
chr9:32441218
|
G | T | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2370+631G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441218 | ||||||
chr9:32441229
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2370+642T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441229 | ||||||
chr9:32441298
|
C | A | 1 | a0001c0002t0016g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2370+711C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441298 | ||||||
chr9:32441319
|
G | C | 1 | a0001c0002t0065g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2370+732G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441319 | ||||||
chr9:32441352
|
C | T | 1 | a0003c0003t0017g0163 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2370+765C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441352 | ||||||
chr9:32441353
|
A | G | 1 | a0001c0002t0065g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2370+766A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441353 | ||||||
chr9:32441472
|
C | T | 1 | a0001c0001t0003g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2370+885C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441472 | ||||||
chr9:32441602
|
ACT | A | 7 | a0001c0001t0016g0109a0001c0001t0016g0111a0001c0001t0016g0118others(4): Show | 7 | HG00280.hp1 NA18961.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2370+1016_2370+101 others(6): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441602 | ||||||
chr9:32441603
|
CTA | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(106): Show | 119 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.2370+1018_2370+101 others(6): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32441603 | |||||
chr9:32441605
|
A | G | 7 | a0001c0001t0016g0109a0001c0001t0016g0111a0001c0001t0016g0118others(4): Show | 7 | HG00280.hp1 NA18961.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2370+1018A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441605 | ||||||
chr9:32441770
|
T | C | 18 | a0001c0002t0038g0301a0001c0002t0038g0328a0001c0002t0083g0300others(15): Show | 18 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2370+1183T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441770 | ||||||
chr9:32441959
|
T | TTAGAAAG others(50): Show |
1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2370+1373_2370+142 others(61): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32441959 | |||||
chr9:32441975
|
C | T | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2370+1388C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32441975 | ||||||
chr9:32442085
|
A | AT | 5 | a0001c0001t0052g0055a0001c0002t0004g0296a0002c0004t0023g0008others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2370+1510dupT | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32442085 | |||||
chr9:32442163
|
G | C | 3 | a0003c0003t0017g0162a0003c0003t0017g0191a0003c0003t0017g0201 | 3 | HG00673.hp2 HG02132.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.2370+1576G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32442163 | ||||||
chr9:32442258
|
G | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(316): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.2370+1671G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32442258 | ||||||
chr9:32442494
|
A | G | 115 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(112): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.2370+1907A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32442494 | ||||||
chr9:32442835
|
C | T | 1 | a0001c0002t0010g0020 | 2 | HG00423.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.2370+2248C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32442835 | ||||||
chr9:32443071
|
T | A | 1 | a0001c0001t0080g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2370+2484T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443071 | ||||||
chr9:32443082
|
T | A | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2370+2495T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443082 | ||||||
chr9:32443095
|
A | C | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2370+2508A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443095 | ||||||
chr9:32443274
|
T | TA | 8 | a0001c0001t0005g0155a0001c0001t0016g0120a0001c0001t0054g0312others(5): Show | 8 | HG00621.hp1 HG02129.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2370+2695dupA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32443274 | |||||
chr9:32443445
|
T | C | 1 | a0001c0001t0014g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2370+2858T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443445 | ||||||
chr9:32443450
|
G | C | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2370+2863G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443450 | ||||||
chr9:32443565
|
A | G | 10 | a0001c0002t0002g0003a0001c0002t0002g0166a0001c0002t0002g0171others(7): Show | 13 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.2370+2978A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443565 | ||||||
chr9:32443660
|
G | A | 7 | a0001c0001t0003g0007a0001c0001t0003g0018a0001c0001t0003g0065others(4): Show | 8 | HG02280.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2370+3073G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443660 | ||||||
chr9:32443669
|
C | T | 4 | a0001c0001t0029g0017a0001c0001t0029g0148a0001c0001t0029g0153others(1): Show | 4 | HG00639.hp1 HG01261.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2370+3082C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443669 | ||||||
chr9:32443901
|
G | A | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2370+3314G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443901 | ||||||
chr9:32443976
|
T | C | 132 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2370+3389T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32443976 | ||||||
chr9:32444027
|
G | A | 1 | a0013c0017t0104g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2370+3440G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444027 | ||||||
chr9:32444056
|
T | TG | 132 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2370+3470dupG | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32444056 | |||||
chr9:32444173
|
G | A | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2370+3586G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444173 | ||||||
chr9:32444248
|
A | G | 1 | a0001c0001t0004g0044 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2370+3661A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444248 | ||||||
chr9:32444553
|
A | AGCATT | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3966_2370+396 others(9): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444553 | ||||||
chr9:32444557
|
G | T | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3970G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444557 | ||||||
chr9:32444561
|
T | A | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3974T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444561 | ||||||
chr9:32444563
|
C | G | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3976C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444563 | ||||||
chr9:32444565
|
C | T | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3978C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444565 | ||||||
chr9:32444567
|
A | G | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3980A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444567 | ||||||
chr9:32444568
|
A | T | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3981A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444568 | ||||||
chr9:32444572
|
C | G | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3985C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444572 | ||||||
chr9:32444573
|
CAG | C | 10 | a0001c0001t0003g0078a0001c0001t0003g0177a0001c0001t0003g0210others(7): Show | 11 | HG02015.hp2 NA18939.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.2370+3987_2370+398 others(6): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444573 | ||||||
chr9:32444952
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2371-3944C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444952 | ||||||
chr9:32444975
|
A | C | 1 | a0001c0006t0003g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2371-3921A>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444975 | ||||||
chr9:32444976
|
T | C | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2371-3920T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444976 | ||||||
chr9:32444980
|
A | G | 116 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(113): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.2371-3916A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444980 | ||||||
chr9:32444996
|
A | G | 116 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(113): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.2371-3900A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32444996 | ||||||
chr9:32445043
|
C | T | 1 | a0001c0001t0074g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2371-3853C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445043 | ||||||
chr9:32445096
|
G | A | 1 | a0001c0001t0019g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2371-3800G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445096 | ||||||
chr9:32445137
|
C | T | 4 | a0001c0002t0008g0235a0001c0002t0008g0236a0001c0002t0008g0285others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371-3759C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445137 | ||||||
chr9:32445235
|
CTGGTCCT others(14): Show |
C | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3656_2371-363 others(25): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32445235 | |||||
chr9:32445261
|
A | G | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3635A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445261 | ||||||
chr9:32445269
|
A | G | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3627A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445269 | ||||||
chr9:32445271
|
T | G | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3625T>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445271 | ||||||
chr9:32445277
|
C | G | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3619C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445277 | ||||||
chr9:32445343
|
G | T | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3553G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445343 | ||||||
chr9:32445454
|
T | A | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3442T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445454 | ||||||
chr9:32445455
|
G | A | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3441G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445455 | ||||||
chr9:32445456
|
A | G | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3440A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445456 | ||||||
chr9:32445469
|
C | A | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3427C>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445469 | ||||||
chr9:32445475
|
T | C | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3421T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445475 | ||||||
chr9:32445477
|
ATTGCCTC others(22): Show |
A | 1 | a0001c0001t0016g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2371-3416_2371-338 others(33): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr9 | 32445477 | |||||
chr9:32445964
|
G | A | 1 | a0001c0002t0004g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2371-2932G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445964 | ||||||
chr9:32445995
|
T | C | 1 | a0001c0001t0078g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2371-2901T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32445995 | ||||||
chr9:32446019
|
T | A | 1 | a0001c0002t0004g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2371-2877T>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446019 | ||||||
chr9:32446087
|
C | T | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2371-2809C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446087 | ||||||
chr9:32446352
|
G | T | 1 | a0001c0002t0004g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2371-2544G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446352 | ||||||
chr9:32446376
|
A | G | 3 | a0004c0009t0024g0198a0004c0009t0051g0084a0004c0027t0024g0215 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2371-2520A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446376 | ||||||
chr9:32446509
|
G | A | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2371-2387G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446509 | ||||||
chr9:32446739
|
T | C | 1 | a0001c0001t0069g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2371-2157T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446739 | ||||||
chr9:32446909
|
C | G | 1 | a0013c0017t0104g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2371-1987C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446909 | ||||||
chr9:32446986
|
G | A | 1 | a0001c0001t0113g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2371-1910G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32446986 | ||||||
chr9:32447167
|
A | G | 8 | a0001c0011t0109g0140a0001c0011t0110g0141a0001c0019t0112g0138others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2371-1729A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447167 | ||||||
chr9:32447259
|
T | C | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2371-1637T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447259 | ||||||
chr9:32447260
|
G | A | 1 | a0001c0019t0112g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2371-1636G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447260 | ||||||
chr9:32447295
|
A | T | 1 | a0012c0028t0007g0266 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2371-1601A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447295 | ||||||
chr9:32447296
|
T | C | 1 | a0001c0019t0112g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2371-1600T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447296 | ||||||
chr9:32447415
|
CA | C | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2371-1480delA | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447415 | ||||||
chr9:32447417
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2371-1479G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447417 | ||||||
chr9:32447589
|
C | T | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2371-1307C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447589 | ||||||
chr9:32447597
|
T | C | 1 | a0001c0001t0003g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2371-1299T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447597 | ||||||
chr9:32447670
|
G | C | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2371-1226G>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447670 | ||||||
chr9:32447739
|
G | A | 4 | a0001c0001t0004g0044a0001c0001t0004g0183a0001c0001t0004g0199others(1): Show | 4 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371-1157G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447739 | ||||||
chr9:32447816
|
G | A | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2371-1080G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447816 | ||||||
chr9:32447912
|
C | T | 1 | a0013c0017t0104g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2371-984C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447912 | ||||||
chr9:32447924
|
C | G | 7 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2371-972C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32447924 | ||||||
chr9:32448029
|
C | T | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2371-867C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448029 | ||||||
chr9:32448038
|
G | A | 31 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0022others(28): Show | 33 | HG00597.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.2371-858G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448038 | ||||||
chr9:32448044
|
A | G | 1 | a0001c0006t0105g0315 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2371-852A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448044 | ||||||
chr9:32448044
|
A | T | 1 | a0001c0023t0066g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2371-852A>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448044 | ||||||
chr9:32448360
|
C | T | 45 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0022others(42): Show | 48 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2371-536C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448360 | ||||||
chr9:32448438
|
A | G | 12 | a0001c0001t0007g0030a0001c0001t0007g0039a0001c0001t0007g0054others(9): Show | 13 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2371-458A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448438 | ||||||
chr9:32448539
|
G | A | 1 | a0001c0001t0091g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2371-357G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448539 | ||||||
chr9:32448573
|
G | A | 15 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(12): Show | 15 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2371-323G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448573 | ||||||
chr9:32448656
|
C | G | 3 | a0004c0009t0024g0198a0004c0009t0051g0084a0004c0027t0024g0215 | 3 | HG03139.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2371-240C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448656 | ||||||
chr9:32448705
|
A | G | 7 | a0001c0011t0109g0140a0001c0011t0110g0141a0002c0007t0031g0094others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2371-191A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448705 | ||||||
chr9:32448747
|
T | C | 139 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(136): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2371-149T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448747 | ||||||
chr9:32448764
|
C | G | 4 | a0001c0002t0004g0241a0001c0002t0004g0272a0001c0002t0056g0250others(1): Show | 4 | NA18959.hp2 NA18969.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.2371-132C>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448764 | ||||||
chr9:32448799
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0134a0001c0001t0005g0306others(2): Show | 5 | HG02132.hp1 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2371-97C>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448799 | ||||||
chr9:32448857
|
G | T | 7 | a0001c0001t0001g0238a0001c0002t0027g0303a0001c0002t0027g0305others(4): Show | 7 | HG01175.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2371-39G>T | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 19/20 | chr9 | 32448857 | ||||||
chr9:32449246
|
T | C | 194 | a0001c0001t0001g0238a0001c0001t0002g0149a0001c0001t0002g0168others(191): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2556+165T>C | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/20 | chr9 | 32449246 | ||||||
chr9:32449269
|
T | TTTA | 14 | a0001c0008t0032g0086a0001c0008t0032g0326a0001c0010t0028g0066others(11): Show | 14 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2556+189_2556+191d others(5): Show |
ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr9 | 32449269 | |||||
chr9:32449358
|
G | A | 1 | a0001c0001t0005g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2556+277G>A | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/20 | chr9 | 32449358 | ||||||
chr9:32449809
|
A | G | 154 | a0001c0001t0002g0149a0001c0001t0002g0168a0001c0001t0002g0322others(151): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.2557-189A>G | ACO1 | ENSG00000122729.19 | transcript | ENST00000309951.8 | protein_coding | 20/20 | chr9 | 32449809 |