geneid | 123876 |
---|---|
ensemblid | ENSG00000183747.12 |
hgncid | 32017 |
symbol | ACSM2A |
name | acyl-CoA synthetase medium chain family member 2A |
refseq_nuc | NM_001308172.2 |
refseq_prot | NP_001295101.1 |
ensembl_nuc | ENST00000573854.6 |
ensembl_prot | ENSP00000459451.1 |
mane_status | MANE Select |
chr | chr16 |
start | 20451521 |
end | 20487669 |
strand | + |
ver | v1.2 |
region | chr16:20451521-20487669 |
region5000 | chr16:20446521-20492669 |
regionname0 | ACSM2A_chr16_20451521_20487669 |
regionname5000 | ACSM2A_chr16_20446521_20492669 |
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 | 0/0 | 577 | 110 | 19 | 50 | 20 | 8 | 13 | 14 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002 | 0/0 | 577 | 90 | 0 | 8 | 68 | 4 | 10 | 57 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003 | 0/1 | 577 | 71 | 44 | 5 | 13 | 1 | 7 | 12 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0004 | 0/0 | 577 | 51 | 8 | 6 | 31 | 1 | 5 | 24 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005 | 1/0 | 577 | 34 | 1 | 4 | 22 | 2 | 4 | 13 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006 | 0/0 | 114 | 34 | 0 | 0 | 33 | 0 | 1 | 29 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0007 | 0/0 | 577 | 12 | 9 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0008 | 0/0 | 577 | 8 | 2 | 3 | 3 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0009 | 0/0 | 577 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0010 | 0/0 | 577 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0011 | 0/0 | 577 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0012 | 0/0 | 577 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0013 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0014 | 0/0 | 69 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0015 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0016 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0017 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0018 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0019 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0020 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0021 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
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 | 0/0 | 1734 | 107 | 17 | 49 | 20 | 8 | 13 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0002 | 0/0 | 1734 | 89 | 0 | 8 | 67 | 4 | 10 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0003 | 0/1 | 1734 | 61 | 35 | 5 | 13 | 1 | 6 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0004 | 0/0 | 1734 | 49 | 6 | 6 | 31 | 1 | 5 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0005 | 1/0 | 1734 | 34 | 1 | 4 | 22 | 2 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0006 | 0/0 | 1734 | 32 | 0 | 0 | 31 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0007 | 0/0 | 1734 | 12 | 9 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0008 | 0/0 | 1734 | 8 | 2 | 3 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0009 | 0/0 | 1734 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0010 | 0/0 | 1734 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0011 | 0/0 | 1734 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0012 | 0/0 | 1734 | 4 | 0 | 0 | 0 | 0 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0013 | 0/0 | 1734 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0014 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0015 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0016 | 0/0 | 1734 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0017 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0018 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0019 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0020 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0021 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0022 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0023 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0024 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0025 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0026 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0027 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0028 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0029 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
c0030 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
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 | 1161 | 142 | 28 | 55 | 33 | 7 | 19 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0002 | 0/0 | 1161 | 117 | 24 | 9 | 73 | 1 | 10 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0003 | 0/1 | 1161 | 82 | 0 | 8 | 58 | 5 | 10 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0004 | 1/0 | 1161 | 17 | 0 | 4 | 9 | 1 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0005 | 0/0 | 1161 | 15 | 15 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0006 | 0/0 | 1161 | 9 | 9 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0007 | 0/0 | 1161 | 8 | 6 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0008 | 0/0 | 1161 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0009 | 0/0 | 1161 | 5 | 0 | 0 | 5 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0010 | 0/0 | 1161 | 5 | 5 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0011 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0012 | 0/0 | 1161 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0013 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0014 | 0/0 | 1161 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0015 | 0/0 | 1161 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0016 | 0/0 | 1161 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0017 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0018 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0019 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0020 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0021 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0022 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0023 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0024 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0025 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0026 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0027 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0028 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0029 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0030 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0031 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
t0032 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
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 | 5 | 0 | 5 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0003 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
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 | 0/0 | 1734 | 107 | 17 | 49 | 20 | 8 | 13 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0017 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0018 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002 | 0/0 | 1734 | 89 | 0 | 8 | 67 | 4 | 10 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0022 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003 | 0/1 | 1734 | 61 | 35 | 5 | 13 | 1 | 6 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0010 | 0/0 | 1734 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0015 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0023 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0026 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0004c0004 | 0/0 | 1734 | 49 | 6 | 6 | 31 | 1 | 5 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0004c0014 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005 | 1/0 | 1734 | 34 | 1 | 4 | 22 | 2 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0006 | 0/0 | 1734 | 32 | 0 | 0 | 31 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0016 | 0/0 | 1734 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0007c0007 | 0/0 | 1734 | 12 | 9 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0008c0008 | 0/0 | 1734 | 8 | 2 | 3 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0009c0009 | 0/0 | 1734 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0010c0012 | 0/0 | 1734 | 4 | 0 | 0 | 0 | 0 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0011c0011 | 0/0 | 1734 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0012c0013 | 0/0 | 1734 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0013c0021 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0014c0020 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0015c0019 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0016c0028 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0017c0030 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0018c0029 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0019c0024 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0020c0027 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0021c0025 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2894 | 91 | 10 | 45 | 17 | 7 | 12 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0004 | 0/0 | 2894 | 6 | 0 | 4 | 0 | 1 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0006 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0010 | 0/0 | 2894 | 5 | 5 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0024 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0025 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0026 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0001t0027 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0017t0001 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0001c0018t0001 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0002 | 0/0 | 2894 | 9 | 0 | 2 | 6 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0003 | 0/0 | 2894 | 63 | 0 | 4 | 48 | 4 | 7 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0007 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0008 | 0/0 | 2894 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0009 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0014 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0015 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0017 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0018 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0021 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0002t0022 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0002c0022t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003t0002 | 0/0 | 2894 | 33 | 19 | 1 | 10 | 0 | 3 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003t0003 | 0/1 | 2894 | 9 | 0 | 4 | 1 | 1 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003t0005 | 0/0 | 2894 | 11 | 11 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003t0007 | 0/0 | 2894 | 5 | 5 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003t0009 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0003t0012 | 0/0 | 2894 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0010t0001 | 0/0 | 2894 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0010t0006 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0015t0001 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0023t0002 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0003c0026t0007 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0004c0004t0002 | 0/0 | 2894 | 47 | 4 | 6 | 31 | 1 | 5 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0004c0004t0013 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0004c0014t0001 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005t0001 | 0/0 | 2894 | 18 | 1 | 3 | 12 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005t0004 | 1/0 | 2894 | 11 | 0 | 0 | 9 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005t0016 | 0/0 | 2894 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005t0029 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005t0030 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0005c0005t0032 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0006t0002 | 0/0 | 2894 | 21 | 0 | 0 | 20 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0006t0003 | 0/0 | 2894 | 7 | 0 | 0 | 7 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0006t0009 | 0/0 | 2894 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0006t0019 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0006c0016t0002 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0007c0007t0001 | 0/0 | 2894 | 7 | 4 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0007c0007t0011 | 0/0 | 2894 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0007c0007t0023 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0007c0007t0028 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0008c0008t0001 | 0/0 | 2894 | 8 | 2 | 3 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0009c0009t0001 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0009c0009t0006 | 0/0 | 2894 | 6 | 6 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0010c0012t0001 | 0/0 | 2894 | 4 | 0 | 0 | 0 | 0 | 4 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0011c0011t0005 | 0/0 | 2894 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0011c0011t0007 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0012c0013t0002 | 0/0 | 2894 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0013c0021t0002 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0014c0020t0003 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0015c0019t0003 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0016c0028t0001 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0017c0030t0031 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0018c0029t0001 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0019c0024t0002 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0020c0027t0020 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
a0021c0025t0005 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | copy fasta | chr16 | 20446521 | 20492669 |
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 | 5 | 0 | 5 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0024g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0025g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0001t0027g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0017t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0017t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0001c0018t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0007g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0014g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0015g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0015g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0017g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0018g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0021g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0002t0022g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0002c0022t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0007g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0009g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0003t0012g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0010t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0015t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0015t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0023t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0003c0026t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0003 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0013g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0004t0013g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0014t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0004c0014t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0016g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0016g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0029g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0030g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0005c0005t0032g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0009g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0009g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0009g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0006t0019g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0016t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0006c0016t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0011g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0023g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0007c0007t0028g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0008c0008t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0009c0009t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0012t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0012t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0010c0012t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0011t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0011t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0011t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0011c0011t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0012c0013t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0012c0013t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0013c0021t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0014c0020t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0015c0019t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0016c0028t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0017c0030t0031g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0018c0029t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0019c0024t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0020c0027t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
a0021c0025t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0016 | g0137 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00140 | hp2 | a0004 | c0004 | t0002 | g0003 | EUR | GBR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0243 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00323 | hp1 | a0005 | c0005 | t0016 | g0138 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00408 | hp1 | a0004 | c0004 | t0002 | g0003 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0240 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00423 | hp1 | a0005 | c0005 | t0001 | g0135 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00438 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00438 | hp2 | a0005 | c0005 | t0001 | g0016 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00544 | hp2 | a0005 | c0005 | t0004 | g0071 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00558 | hp1 | a0001 | c0001 | t0027 | g0153 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00558 | hp2 | a0004 | c0004 | t0002 | g0320 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00609 | hp1 | a0008 | c0008 | t0001 | g0152 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00621 | hp1 | a0004 | c0004 | t0002 | g0328 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00621 | hp2 | a0005 | c0005 | t0001 | g0042 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00673 | hp1 | a0002 | c0002 | t0015 | g0010 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00673 | hp2 | a0006 | c0006 | t0002 | g0036 | EAS | CHS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00733 | hp1 | a0002 | c0002 | t0017 | g0235 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00735 | hp1 | a0005 | c0005 | t0032 | g0132 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00738 | hp1 | a0002 | c0002 | t0018 | g0200 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0252 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG00741 | hp2 | a0008 | c0008 | t0001 | g0189 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01070 | hp1 | a0003 | c0003 | t0003 | g0035 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0351 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01074 | hp1 | a0004 | c0004 | t0002 | g0299 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0244 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01081 | hp1 | a0002 | c0002 | t0003 | g0246 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01081 | hp2 | a0004 | c0004 | t0002 | g0296 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01099 | hp2 | a0008 | c0008 | t0001 | g0015 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01109 | hp2 | a0007 | c0007 | t0001 | g0068 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01168 | hp1 | a0008 | c0008 | t0001 | g0038 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01175 | hp1 | a0005 | c0005 | t0001 | g0139 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01175 | hp2 | a0005 | c0005 | t0001 | g0022 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0234 | AMR | PUR | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01256 | hp1 | a0004 | c0004 | t0002 | g0372 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01258 | hp1 | a0003 | c0003 | t0002 | g0310 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01346 | hp1 | a0001 | c0018 | t0001 | g0043 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01358 | hp1 | a0005 | c0005 | t0001 | g0073 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0380 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0253 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0125 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01496 | hp1 | a0007 | c0007 | t0001 | g0083 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0177 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01516 | hp1 | a0002 | c0002 | t0003 | g0027 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0027 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01884 | hp1 | a0003 | c0003 | t0005 | g0030 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0370 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01928 | hp2 | a0017 | c0030 | t0031 | g0122 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01934 | hp1 | a0007 | c0007 | t0001 | g0102 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01978 | hp1 | a0004 | c0004 | t0002 | g0330 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02015 | hp1 | a0005 | c0005 | t0001 | g0134 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02015 | hp2 | a0003 | c0003 | t0009 | g0309 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02027 | hp1 | a0005 | c0005 | t0030 | g0084 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0205 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02055 | hp2 | a0008 | c0008 | t0001 | g0146 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02056 | hp2 | a0004 | c0004 | t0002 | g0290 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02071 | hp1 | a0006 | c0006 | t0009 | g0356 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02071 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02080 | hp1 | a0002 | c0002 | t0014 | g0025 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02080 | hp2 | a0004 | c0004 | t0002 | g0312 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02083 | hp1 | a0005 | c0005 | t0001 | g0063 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02083 | hp2 | a0006 | c0006 | t0003 | g0035 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02129 | hp1 | a0006 | c0016 | t0002 | g0360 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02129 | hp2 | a0004 | c0004 | t0002 | g0289 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02132 | hp1 | a0005 | c0005 | t0001 | g0062 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02132 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02135 | hp1 | a0002 | c0002 | t0014 | g0025 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02145 | hp1 | a0003 | c0015 | t0001 | g0150 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02145 | hp2 | a0011 | c0011 | t0005 | g0276 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02148 | hp1 | a0004 | c0004 | t0002 | g0323 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02148 | hp2 | a0004 | c0004 | t0002 | g0324 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02165 | hp1 | a0002 | c0002 | t0003 | g0217 | EAS | CDX | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0272 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02257 | hp2 | a0003 | c0003 | t0005 | g0378 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02258 | hp1 | a0009 | c0009 | t0006 | g0165 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02258 | hp2 | a0003 | c0003 | t0002 | g0339 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02280 | hp1 | a0003 | c0003 | t0002 | g0288 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02280 | hp2 | a0003 | c0003 | t0002 | g0034 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02451 | hp1 | a0007 | c0007 | t0001 | g0082 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02451 | hp2 | a0003 | c0003 | t0002 | g0277 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02572 | hp1 | a0003 | c0003 | t0002 | g0284 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02572 | hp2 | a0003 | c0003 | t0002 | g0340 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0202 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0047 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02615 | hp2 | a0003 | c0003 | t0005 | g0286 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02622 | hp1 | a0003 | c0023 | t0002 | g0341 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0046 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02630 | hp1 | a0003 | c0003 | t0007 | g0271 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02630 | hp2 | a0004 | c0004 | t0002 | g0329 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02647 | hp1 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02647 | hp2 | a0003 | c0003 | t0002 | g0283 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02698 | hp1 | a0003 | c0003 | t0002 | g0319 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02698 | hp2 | a0003 | c0003 | t0002 | g0033 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02717 | hp1 | a0003 | c0010 | t0006 | g0163 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02717 | hp2 | a0001 | c0017 | t0001 | g0064 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02723 | hp1 | a0007 | c0007 | t0001 | g0101 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02723 | hp2 | a0003 | c0003 | t0002 | g0034 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02735 | hp1 | a0005 | c0005 | t0001 | g0136 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0198 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02738 | hp1 | a0004 | c0004 | t0002 | g0318 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02818 | hp1 | a0003 | c0003 | t0002 | g0342 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02818 | hp2 | a0009 | c0009 | t0006 | g0023 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02886 | hp1 | a0003 | c0010 | t0001 | g0159 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02895 | hp1 | a0008 | c0008 | t0001 | g0015 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02895 | hp2 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02896 | hp1 | a0003 | c0010 | t0001 | g0162 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0045 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0044 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02897 | hp2 | a0003 | c0003 | t0005 | g0287 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02922 | hp1 | a0003 | c0003 | t0002 | g0371 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02922 | hp2 | a0003 | c0003 | t0005 | g0030 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02965 | hp1 | a0003 | c0003 | t0007 | g0011 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02965 | hp2 | a0007 | c0007 | t0011 | g0085 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02970 | hp1 | a0003 | c0003 | t0007 | g0249 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02970 | hp2 | a0004 | c0004 | t0002 | g0281 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02976 | hp2 | a0003 | c0003 | t0002 | g0355 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03041 | hp1 | a0004 | c0014 | t0001 | g0157 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03041 | hp2 | a0009 | c0009 | t0006 | g0154 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03098 | hp1 | a0004 | c0004 | t0002 | g0279 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03098 | hp2 | a0007 | c0007 | t0001 | g0103 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03130 | hp1 | a0007 | c0007 | t0023 | g0104 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03130 | hp2 | a0011 | c0011 | t0005 | g0274 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03139 | hp1 | a0007 | c0007 | t0028 | g0105 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03139 | hp2 | a0003 | c0003 | t0005 | g0176 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03195 | hp1 | a0007 | c0007 | t0001 | g0005 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03195 | hp2 | a0003 | c0010 | t0001 | g0161 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03209 | hp1 | a0004 | c0014 | t0001 | g0160 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03209 | hp2 | a0003 | c0003 | t0005 | g0175 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03225 | hp1 | a0020 | c0027 | t0020 | g0280 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03225 | hp2 | a0003 | c0003 | t0007 | g0011 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03453 | hp1 | a0003 | c0003 | t0002 | g0375 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03453 | hp2 | a0003 | c0010 | t0001 | g0158 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03486 | hp1 | a0003 | c0003 | t0002 | g0037 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03486 | hp2 | a0009 | c0009 | t0006 | g0166 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03490 | hp1 | a0010 | c0012 | t0001 | g0014 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03490 | hp2 | a0003 | c0003 | t0002 | g0033 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03491 | hp1 | a0016 | c0028 | t0001 | g0092 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0257 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03492 | hp1 | a0010 | c0012 | t0001 | g0014 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03516 | hp1 | a0007 | c0007 | t0011 | g0005 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03516 | hp2 | a0001 | c0001 | t0026 | g0061 | AFR | ESN | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03540 | hp1 | a0021 | c0025 | t0005 | g0291 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0357 | AFR | GWD | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03579 | hp2 | a0003 | c0003 | t0005 | g0258 | AFR | MSL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0206 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03669 | hp2 | a0004 | c0004 | t0002 | g0317 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03688 | hp1 | a0005 | c0005 | t0001 | g0054 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03688 | hp2 | a0005 | c0005 | t0004 | g0067 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03704 | hp2 | a0003 | c0026 | t0007 | g0170 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03710 | hp1 | a0002 | c0002 | t0003 | g0237 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03831 | hp1 | a0003 | c0003 | t0012 | g0172 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03831 | hp2 | a0006 | c0006 | t0002 | g0338 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03927 | hp1 | a0010 | c0012 | t0001 | g0051 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03927 | hp2 | a0002 | c0002 | t0007 | g0241 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG03942 | hp2 | a0015 | c0019 | t0003 | g0010 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04115 | hp2 | a0002 | c0002 | t0021 | g0232 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04184 | hp1 | a0010 | c0012 | t0001 | g0052 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04184 | hp2 | a0004 | c0004 | t0002 | g0300 | SAS | BEB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0254 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0248 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04204 | hp2 | a0004 | c0004 | t0002 | g0327 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04228 | hp1 | a0004 | c0004 | t0002 | g0326 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0201 | SAS | STU | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18522 | hp1 | a0003 | c0010 | t0006 | g0164 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18522 | hp2 | a0001 | c0017 | t0001 | g0065 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18612 | hp1 | a0008 | c0008 | t0001 | g0190 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18612 | hp2 | a0005 | c0005 | t0001 | g0075 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18747 | hp1 | a0002 | c0002 | t0003 | g0260 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18747 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | CHB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18940 | hp2 | a0002 | c0002 | t0008 | g0207 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18941 | hp1 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0245 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18942 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18942 | hp2 | a0006 | c0006 | t0002 | g0348 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18943 | hp1 | a0005 | c0005 | t0001 | g0078 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18943 | hp2 | a0003 | c0003 | t0002 | g0314 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18945 | hp1 | a0004 | c0004 | t0002 | g0032 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18946 | hp1 | a0006 | c0006 | t0002 | g0353 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18946 | hp2 | a0005 | c0005 | t0001 | g0144 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18948 | hp2 | a0002 | c0002 | t0008 | g0009 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18949 | hp1 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18949 | hp2 | a0006 | c0006 | t0002 | g0349 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0223 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18950 | hp2 | a0004 | c0004 | t0002 | g0334 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18951 | hp1 | a0003 | c0003 | t0002 | g0173 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18951 | hp2 | a0002 | c0002 | t0003 | g0216 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0228 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18953 | hp1 | a0006 | c0006 | t0003 | g0012 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0208 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18954 | hp1 | a0006 | c0006 | t0002 | g0354 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18956 | hp1 | a0006 | c0006 | t0002 | g0367 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18957 | hp1 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18957 | hp2 | a0006 | c0006 | t0003 | g0012 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18959 | hp1 | a0006 | c0006 | t0002 | g0036 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18959 | hp2 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18960 | hp1 | a0004 | c0004 | t0002 | g0313 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18960 | hp2 | a0002 | c0002 | t0003 | g0197 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18961 | hp1 | a0004 | c0004 | t0002 | g0298 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18961 | hp2 | a0006 | c0006 | t0009 | g0374 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18962 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18964 | hp1 | a0005 | c0005 | t0004 | g0041 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18964 | hp2 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0265 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18965 | hp2 | a0005 | c0005 | t0001 | g0140 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18966 | hp1 | a0002 | c0002 | t0003 | g0233 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18966 | hp2 | a0005 | c0005 | t0004 | g0074 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18967 | hp2 | a0002 | c0002 | t0008 | g0210 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18968 | hp1 | a0006 | c0006 | t0002 | g0270 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18969 | hp1 | a0001 | c0001 | t0024 | g0169 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18969 | hp2 | a0012 | c0013 | t0002 | g0229 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18970 | hp2 | a0005 | c0005 | t0004 | g0131 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18971 | hp1 | a0003 | c0003 | t0002 | g0331 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0305 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18972 | hp1 | a0004 | c0004 | t0002 | g0315 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18972 | hp2 | a0002 | c0002 | t0003 | g0268 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18974 | hp1 | a0002 | c0002 | t0008 | g0009 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18974 | hp2 | a0006 | c0006 | t0002 | g0368 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0303 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18978 | hp1 | a0006 | c0006 | t0002 | g0361 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18978 | hp2 | a0006 | c0006 | t0002 | g0343 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0238 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18979 | hp2 | a0006 | c0006 | t0002 | g0350 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18982 | hp1 | a0005 | c0005 | t0004 | g0077 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18987 | hp1 | a0002 | c0002 | t0003 | g0224 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18987 | hp2 | a0004 | c0004 | t0002 | g0337 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18988 | hp2 | a0004 | c0004 | t0002 | g0295 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18989 | hp1 | a0002 | c0002 | t0003 | g0230 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18989 | hp2 | a0004 | c0004 | t0002 | g0304 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18990 | hp1 | a0004 | c0004 | t0002 | g0301 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0218 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18991 | hp2 | a0005 | c0005 | t0004 | g0079 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18992 | hp1 | a0004 | c0004 | t0002 | g0335 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0267 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18994 | hp2 | a0006 | c0006 | t0002 | g0347 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18995 | hp1 | a0004 | c0004 | t0002 | g0321 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18997 | hp1 | a0005 | c0005 | t0004 | g0130 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18997 | hp2 | a0006 | c0006 | t0003 | g0352 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18998 | hp1 | a0002 | c0022 | t0003 | g0225 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18998 | hp2 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18999 | hp1 | a0003 | c0003 | t0002 | g0306 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18999 | hp2 | a0006 | c0016 | t0002 | g0358 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19000 | hp1 | a0006 | c0006 | t0002 | g0369 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19000 | hp2 | a0005 | c0005 | t0004 | g0076 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0261 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19002 | hp2 | a0002 | c0002 | t0003 | g0211 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19004 | hp2 | a0002 | c0002 | t0015 | g0256 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19006 | hp1 | a0002 | c0002 | t0003 | g0377 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19006 | hp2 | a0006 | c0006 | t0003 | g0373 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19007 | hp1 | a0005 | c0005 | t0001 | g0016 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19007 | hp2 | a0006 | c0006 | t0002 | g0366 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19010 | hp1 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19010 | hp2 | a0006 | c0006 | t0009 | g0346 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0247 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19011 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19012 | hp1 | a0004 | c0004 | t0002 | g0032 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19012 | hp2 | a0004 | c0004 | t0002 | g0297 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19030 | hp1 | a0009 | c0009 | t0006 | g0023 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19030 | hp2 | a0007 | c0007 | t0011 | g0005 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19043 | hp1 | a0003 | c0003 | t0002 | g0282 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19043 | hp2 | a0011 | c0011 | t0007 | g0273 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19054 | hp1 | a0006 | c0006 | t0002 | g0037 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19054 | hp2 | a0012 | c0013 | t0002 | g0236 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19056 | hp1 | a0006 | c0006 | t0003 | g0012 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19056 | hp2 | a0002 | c0002 | t0008 | g0209 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19058 | hp1 | a0005 | c0005 | t0004 | g0072 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19058 | hp2 | a0003 | c0003 | t0002 | g0308 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0307 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19062 | hp1 | a0019 | c0024 | t0002 | g0311 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19062 | hp2 | a0004 | c0004 | t0002 | g0293 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19064 | hp1 | a0004 | c0004 | t0002 | g0376 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19064 | hp2 | a0003 | c0003 | t0012 | g0171 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19065 | hp1 | a0004 | c0004 | t0002 | g0325 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0266 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0264 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19066 | hp2 | a0004 | c0004 | t0002 | g0322 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19067 | hp1 | a0002 | c0002 | t0003 | g0231 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19067 | hp2 | a0006 | c0006 | t0002 | g0365 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19068 | hp1 | a0006 | c0006 | t0003 | g0359 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19068 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19070 | hp2 | a0005 | c0005 | t0001 | g0133 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19072 | hp1 | a0003 | c0003 | t0002 | g0332 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19072 | hp2 | a0002 | c0002 | t0003 | g0263 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19075 | hp1 | a0013 | c0021 | t0002 | g0212 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19075 | hp2 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19076 | hp1 | a0002 | c0002 | t0008 | g0009 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19079 | hp1 | a0002 | c0002 | t0022 | g0195 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19080 | hp1 | a0006 | c0006 | t0002 | g0362 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19082 | hp1 | a0006 | c0006 | t0002 | g0364 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19082 | hp2 | a0004 | c0004 | t0002 | g0333 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19083 | hp1 | a0002 | c0002 | t0008 | g0193 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19083 | hp2 | a0002 | c0002 | t0009 | g0259 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19084 | hp1 | a0018 | c0029 | t0001 | g0070 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19086 | hp2 | a0006 | c0006 | t0019 | g0344 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19087 | hp1 | a0004 | c0004 | t0002 | g0316 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19087 | hp2 | a0014 | c0020 | t0003 | g0002 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19088 | hp1 | a0004 | c0004 | t0002 | g0302 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19088 | hp2 | a0004 | c0004 | t0002 | g0292 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19089 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19089 | hp2 | a0001 | c0001 | t0025 | g0055 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19090 | hp1 | a0004 | c0004 | t0002 | g0336 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19090 | hp2 | a0008 | c0008 | t0001 | g0181 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19091 | hp1 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19091 | hp2 | a0006 | c0006 | t0002 | g0363 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19240 | hp1 | a0003 | c0003 | t0002 | g0250 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA19240 | hp2 | a0003 | c0003 | t0007 | g0011 | AFR | YRI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0269 | AFR | ASW | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20752 | hp1 | a0003 | c0003 | t0003 | g0251 | EUR | TSI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0199 | SAS | GIH | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20905 | hp2 | a0005 | c0005 | t0029 | g0080 | SAS | GIH | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01123 | hp1 | a0002 | c0002 | t0003 | g0242 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0239 | AMR | CLM | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02109 | hp1 | a0003 | c0003 | t0005 | g0285 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02109 | hp2 | a0009 | c0009 | t0006 | g0156 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02486 | hp2 | a0003 | c0015 | t0001 | g0151 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02559 | hp1 | a0004 | c0004 | t0013 | g0278 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0345 | AFR | ACB | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG06807 | hp1 | a0005 | c0005 | t0001 | g0022 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
HG06807 | hp2 | a0009 | c0009 | t0001 | g0167 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA18955 | hp2 | a0002 | c0002 | t0003 | g0226 | EAS | JPT | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20300 | hp1 | a0011 | c0011 | t0005 | g0275 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA20300 | hp2 | a0004 | c0004 | t0013 | g0379 | AFR | USA | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0003 | g0196 | REF | REF | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
homoSapiens_grch38 | hp1 | a0005 | c0005 | t0004 | g0040 | REF | REF | ACSM2A_chr16_20446521_20492669 | ACSM2A | chr16 | 20446521 | 20492669 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20460128
|
G | A | 5 | a0002a0012a0013others(2): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
missense_variant | MODERATE | c.14G>A | p.Arg5Gln | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 183/2894 | 14/1734 | 5/577 | chr16 | 20460128 | ||
chr16:20460139
|
G | A | 1 | a0015 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.25G>A | p.Gly9Arg | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 194/2894 | 25/1734 | 9/577 | chr16 | 20460139 | ||
chr16:20460165
|
G | C | 1 | a0009 | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
missense_variant | MODERATE | c.51G>C | p.Gln17His | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 220/2894 | 51/1734 | 17/577 | chr16 | 20460165 | ||
chr16:20465530
|
T | C | 12 | a0002a0003a0004others(9): Show | 264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
missense_variant | MODERATE | c.191T>C | p.Leu64Pro | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 360/2894 | 191/1734 | 64/577 | chr16 | 20465530 | ||
chr16:20465549
|
G | A | 1 | a0014 | 1 | NA19087.hp2 | stop_gained | HIGH | c.210G>A | p.Trp70* | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 379/2894 | 210/1734 | 70/577 | chr16 | 20465549 | ||
chr16:20465571
|
G | A | 1 | a0010 | 4 | HG03490.hp1 HG03492.hp1 HG03927.hp1 others(1): Show |
missense_variant | MODERATE | c.232G>A | p.Glu78Lys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 401/2894 | 232/1734 | 78/577 | chr16 | 20465571 | ||
chr16:20465652
|
C | T | 1 | a0011 | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
missense_variant | MODERATE | c.313C>T | p.Arg105Cys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 482/2894 | 313/1734 | 105/577 | chr16 | 20465652 | ||
chr16:20465673
|
G | A | 1 | a0013 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.334G>A | p.Val112Met | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 503/2894 | 334/1734 | 112/577 | chr16 | 20465673 | ||
chr16:20465682
|
C | T | 1 | a0006 | 34 | HG00673.hp2 HG02071.hp1 HG02083.hp2 others(31): Show |
stop_gained | HIGH | c.343C>T | p.Arg115* | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 512/2894 | 343/1734 | 115/577 | chr16 | 20465682 | ||
chr16:20469575
|
T | A | 1 | a0019 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.452T>A | p.Met151Lys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/14 | 621/2894 | 452/1734 | 151/577 | chr16 | 20469575 | ||
chr16:20471605
|
G | C | 1 | a0016 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.810G>C | p.Leu270Phe | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/14 | 979/2894 | 810/1734 | 270/577 | chr16 | 20471605 | ||
chr16:20471606
|
T | G | 1 | a0021 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.811T>G | p.Cys271Gly | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/14 | 980/2894 | 811/1734 | 271/577 | chr16 | 20471606 | ||
chr16:20480604
|
G | A | 1 | a0007 | 12 | HG01109.hp2 HG01496.hp1 HG01934.hp1 others(9): Show |
missense_variant | MODERATE | c.1313G>A | p.Arg438Gln | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/14 | 1482/2894 | 1313/1734 | 438/577 | chr16 | 20480604 | ||
chr16:20480678
|
A | G | 18 | a0001a0002a0003others(15): Show | 397 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(394): Show |
missense_variant | MODERATE | c.1387A>G | p.Asn463Asp | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/14 | 1556/2894 | 1387/1734 | 463/577 | chr16 | 20480678 | ||
chr16:20483076
|
G | A | 1 | a0017 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1528G>A | p.Val510Ile | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1697/2894 | 1528/1734 | 510/577 | chr16 | 20483076 | ||
chr16:20483086
|
C | T | 6 | a0004a0006a0008others(3): Show | 65 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(62): Show |
missense_variant | MODERATE | c.1538C>T | p.Ser513Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1707/2894 | 1538/1734 | 513/577 | chr16 | 20483086 | ||
chr16:20486625
|
G | A | 1 | a0017 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1681G>A | p.Ala561Thr | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1850/2894 | 1681/1734 | 561/577 | chr16 | 20486625 | ||
chr16:20486674
|
A | G | 1 | a0020 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1730A>G | p.Gln577Arg | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1899/2894 | 1730/1734 | 577/577 | chr16 | 20486674 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20460120
|
T | C | 1 | a0001c0018 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.6T>C | p.His2His | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 175/2894 | 6/1734 | 2/577 | chr16 | 20460120 | ||
chr16:20460273
|
C | T | 1 | a0002c0022 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.159C>T | p.His53His | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/14 | 328/2894 | 159/1734 | 53/577 | chr16 | 20460273 | ||
chr16:20465567
|
G | A | 1 | a0003c0023 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.228G>A | p.Gly76Gly | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/14 | 397/2894 | 228/1734 | 76/577 | chr16 | 20465567 | ||
chr16:20475403
|
C | T | 1 | a0003c0015 | 2 | HG02145.hp1 HG02486.hp2 |
synonymous_variant | LOW | c.936C>T | p.Pro312Pro | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/14 | 1105/2894 | 936/1734 | 312/577 | chr16 | 20475403 | ||
chr16:20475711
|
C | T | 1 | a0001c0017 | 2 | HG02717.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.1036C>T | p.Leu346Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/14 | 1205/2894 | 1036/1734 | 346/577 | chr16 | 20475711 | ||
chr16:20477374
|
A | G | 16 | a0002c0002a0002c0022a0003c0003others(13): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
synonymous_variant | LOW | c.1104A>G | p.Leu368Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/14 | 1273/2894 | 1104/1734 | 368/577 | chr16 | 20477374 | ||
chr16:20480885
|
G | A | 1 | a0003c0026 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1473G>A | p.Thr491Thr | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/14 | 1642/2894 | 1473/1734 | 491/577 | chr16 | 20480885 | ||
chr16:20483078
|
C | A | 1 | a0017c0030 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1530C>A | p.Val510Val | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1699/2894 | 1530/1734 | 510/577 | chr16 | 20483078 | ||
chr16:20483096
|
G | A | 1 | a0017c0030 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1548G>A | p.Leu516Leu | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/14 | 1717/2894 | 1548/1734 | 516/577 | chr16 | 20483096 | ||
chr16:20486630
|
G | A | 1 | a0017c0030 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1686G>A | p.Lys562Lys | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1855/2894 | 1686/1734 | 562/577 | chr16 | 20486630 | ||
chr16:20486675
|
G | A | 1 | a0020c0027 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1731G>A | p.Gln577Gln | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 1900/2894 | 1731/1734 | 577/577 | chr16 | 20486675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20451602
|
G | A | 36 | a0002c0002t0002a0002c0002t0003a0002c0002t0007others(33): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | 8513 | chr16 | 20451602 | |||||
chr16:20451631
|
G | A | 1 | a0002c0002t0017 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | 8484 | chr16 | 20451631 | |||||
chr16:20451641
|
C | T | 2 | a0005c0005t0016a0005c0005t0032 | 3 | HG00099.hp1 HG00323.hp1 HG00735.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | chr16 | 20451641 | ||||||
chr16:20451653
|
T | C | 1 | a0002c0002t0018 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/14 | 8462 | chr16 | 20451653 | |||||
chr16:20486680
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 2 | chr16 | 20486680 | |||||
chr16:20486682
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 4 | chr16 | 20486682 | |||||
chr16:20486687
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 9 | chr16 | 20486687 | |||||
chr16:20486709
|
C | T | 3 | a0003c0003t0005a0011c0011t0005a0021c0025t0005 | 15 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 31 | chr16 | 20486709 | |||||
chr16:20486738
|
C | A | 1 | a0007c0007t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 60 | chr16 | 20486738 | |||||
chr16:20486749
|
C | A | 2 | a0001c0001t0024a0017c0030t0031 | 2 | HG01928.hp2 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 71 | chr16 | 20486749 | |||||
chr16:20486757
|
T | G | 50 | a0001c0001t0001a0001c0001t0006a0001c0001t0024others(47): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*79T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 79 | chr16 | 20486757 | |||||
chr16:20486775
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 97 | chr16 | 20486775 | |||||
chr16:20486782
|
A | G | 2 | a0002c0002t0021a0005c0005t0029 | 2 | HG04115.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*104A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 104 | chr16 | 20486782 | |||||
chr16:20486788
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 110 | chr16 | 20486788 | |||||
chr16:20486805
|
T | C | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*127T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 127 | chr16 | 20486805 | |||||
chr16:20486824
|
T | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 146 | chr16 | 20486824 | |||||
chr16:20486829
|
C | T | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*151C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 151 | chr16 | 20486829 | |||||
chr16:20486839
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 161 | chr16 | 20486839 | |||||
chr16:20486846
|
G | T | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 168 | chr16 | 20486846 | |||||
chr16:20486897
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 219 | chr16 | 20486897 | |||||
chr16:20486938
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 260 | chr16 | 20486938 | |||||
chr16:20486970
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 292 | chr16 | 20486970 | |||||
chr16:20486971
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 293 | chr16 | 20486971 | |||||
chr16:20486976
|
G | A | 1 | a0001c0001t0025 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*298G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 298 | chr16 | 20486976 | |||||
chr16:20486977
|
A | C | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 299 | chr16 | 20486977 | |||||
chr16:20487006
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 328 | chr16 | 20487006 | |||||
chr16:20487012
|
A | C | 1 | a0020c0027t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 334 | chr16 | 20487012 | |||||
chr16:20487026
|
G | T | 2 | a0004c0004t0013a0020c0027t0020 | 3 | HG02559.hp1 HG03225.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*348G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 348 | chr16 | 20487026 | |||||
chr16:20487061
|
A | T | 2 | a0002c0002t0015a0005c0005t0030 | 3 | HG00673.hp1 HG02027.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 383 | chr16 | 20487061 | |||||
chr16:20487069
|
A | T | 1 | a0020c0027t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 391 | chr16 | 20487069 | |||||
chr16:20487078
|
C | A | 50 | a0001c0001t0001a0001c0001t0006a0001c0001t0024others(47): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*400C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 400 | chr16 | 20487078 | |||||
chr16:20487131
|
C | G | 1 | a0001c0001t0010 | 5 | HG02615.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*453C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 453 | chr16 | 20487131 | |||||
chr16:20487180
|
T | G | 1 | a0020c0027t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*502T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 502 | chr16 | 20487180 | |||||
chr16:20487182
|
G | T | 9 | a0001c0001t0006a0002c0002t0007a0003c0003t0007others(6): Show | 20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*504G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 504 | chr16 | 20487182 | |||||
chr16:20487222
|
A | C | 2 | a0003c0003t0012a0017c0030t0031 | 3 | HG01928.hp2 HG03831.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*544A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 544 | chr16 | 20487222 | |||||
chr16:20487241
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 563 | chr16 | 20487241 | |||||
chr16:20487249
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 571 | chr16 | 20487249 | |||||
chr16:20487268
|
T | C | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 590 | chr16 | 20487268 | |||||
chr16:20487278
|
T | C | 1 | a0002c0002t0008 | 7 | NA18940.hp2 NA18948.hp2 NA18967.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*600T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 600 | chr16 | 20487278 | |||||
chr16:20487295
|
G | C | 3 | a0002c0002t0009a0003c0003t0009a0006c0006t0009 | 5 | HG02015.hp2 HG02071.hp1 NA18961.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*617G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 617 | chr16 | 20487295 | |||||
chr16:20487334
|
C | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 656 | chr16 | 20487334 | |||||
chr16:20487335
|
C | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*657C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 657 | chr16 | 20487335 | |||||
chr16:20487340
|
C | T | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 662 | chr16 | 20487340 | |||||
chr16:20487343
|
C | T | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 665 | chr16 | 20487343 | |||||
chr16:20487349
|
A | T | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 671 | chr16 | 20487349 | |||||
chr16:20487353
|
C | A | 1 | a0006c0006t0019 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 675 | chr16 | 20487353 | |||||
chr16:20487358
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*680A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 680 | chr16 | 20487358 | |||||
chr16:20487394
|
T | C | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 716 | chr16 | 20487394 | |||||
chr16:20487414
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 736 | chr16 | 20487414 | |||||
chr16:20487415
|
C | T | 1 | a0007c0007t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 737 | chr16 | 20487415 | |||||
chr16:20487423
|
C | T | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 745 | chr16 | 20487423 | |||||
chr16:20487434
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 756 | chr16 | 20487434 | |||||
chr16:20487458
|
C | T | 2 | a0001c0001t0027a0017c0030t0031 | 2 | HG00558.hp1 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*780C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 780 | chr16 | 20487458 | |||||
chr16:20487494
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*816A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 816 | chr16 | 20487494 | |||||
chr16:20487502
|
T | C | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*824T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 824 | chr16 | 20487502 | |||||
chr16:20487503
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 825 | chr16 | 20487503 | |||||
chr16:20487519
|
G | A | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 841 | chr16 | 20487519 | |||||
chr16:20487519
|
G | T | 1 | a0002c0002t0014 | 2 | HG02080.hp1 HG02135.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 841 | chr16 | 20487519 | |||||
chr16:20487574
|
C | A | 2 | a0001c0001t0026a0017c0030t0031 | 2 | HG01928.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*896C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 896 | chr16 | 20487574 | |||||
chr16:20487580
|
C | T | 1 | a0002c0002t0022 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*902C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 902 | chr16 | 20487580 | |||||
chr16:20487607
|
T | C | 2 | a0007c0007t0011a0017c0030t0031 | 4 | HG01928.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*929T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 929 | chr16 | 20487607 | |||||
chr16:20487620
|
A | G | 1 | a0017c0030t0031 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 14/14 | 942 | chr16 | 20487620 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:20451741
|
CT | C | 2 | a0001c0001t0001g0013a0008c0008t0001g0038 | 3 | HG01168.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-9+64delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20451741 | |||||
chr16:20451776
|
C | T | 1 | a0002c0002t0002g0380 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-9+95C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451776 | ||||||
chr16:20451781
|
C | T | 2 | a0003c0003t0005g0378a0004c0004t0013g0379 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+100C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451781 | ||||||
chr16:20451864
|
C | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0024others(236): Show | 273 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-9+183C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451864 | ||||||
chr16:20451888
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0024g0169 | 2 | NA18955.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-9+207C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451888 | ||||||
chr16:20451918
|
G | T | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+237G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451918 | ||||||
chr16:20451919
|
G | T | 122 | a0003c0003t0002g0033a0003c0003t0002g0034a0003c0003t0002g0037others(119): Show | 134 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-9+238G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451919 | ||||||
chr16:20451920
|
G | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-9+239G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451920 | ||||||
chr16:20451956
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9+275T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451956 | ||||||
chr16:20451974
|
G | A | 7 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(4): Show | 7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+293G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20451974 | ||||||
chr16:20452032
|
T | G | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+351T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452032 | ||||||
chr16:20452081
|
A | G | 384 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(381): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.-9+400A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452081 | ||||||
chr16:20452111
|
A | G | 213 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(210): Show | 240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-9+430A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452111 | ||||||
chr16:20452113
|
T | C | 4 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0012g0171others(1): Show | 4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+432T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452113 | ||||||
chr16:20452132
|
T | A | 1 | a0004c0004t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9+451T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452132 | ||||||
chr16:20452259
|
A | C | 5 | a0002c0002t0003g0028a0002c0002t0003g0029a0002c0002t0003g0267others(2): Show | 7 | NA18959.hp2 NA18970.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+578A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452259 | ||||||
chr16:20452368
|
A | C | 236 | a0001c0001t0001g0155a0002c0002t0002g0199a0002c0002t0002g0204others(233): Show | 264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.-9+687A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452368 | ||||||
chr16:20452423
|
G | C | 1 | a0006c0006t0002g0270 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-9+742G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452423 | ||||||
chr16:20452482
|
A | T | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+801A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452482 | ||||||
chr16:20452483
|
T | A | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+802T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452483 | ||||||
chr16:20452484
|
A | T | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+803A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452484 | ||||||
chr16:20452487
|
CTGTATAT others(13): Show |
C | 1 | a0002c0002t0003g0194 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+823_-9+842delGT others(18): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20452487 | |||||
chr16:20452511
|
A | G | 46 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0339others(43): Show | 50 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-9+830A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452511 | ||||||
chr16:20452562
|
G | A | 222 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(219): Show | 249 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-9+881G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452562 | ||||||
chr16:20452567
|
T | C | 2 | a0003c0003t0002g0272a0003c0003t0007g0271 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-9+886T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452567 | ||||||
chr16:20452583
|
A | T | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+902A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452583 | ||||||
chr16:20452623
|
C | T | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+942C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452623 | ||||||
chr16:20452625
|
A | C | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+944A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452625 | ||||||
chr16:20452626
|
T | A | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+945T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452626 | ||||||
chr16:20452699
|
A | G | 1 | a0004c0004t0002g0337 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-9+1018A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452699 | ||||||
chr16:20452710
|
A | G | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+1029A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452710 | ||||||
chr16:20452715
|
T | A | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1034T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452715 | ||||||
chr16:20452745
|
T | C | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-9+1064T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452745 | ||||||
chr16:20452746
|
G | A | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-9+1065G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452746 | ||||||
chr16:20452794
|
G | A | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+1113G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452794 | ||||||
chr16:20452917
|
C | G | 50 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(47): Show | 56 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-9+1236C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20452917 | ||||||
chr16:20453012
|
G | A | 1 | a0005c0005t0004g0041 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-9+1331G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453012 | ||||||
chr16:20453026
|
A | C | 2 | a0001c0001t0027g0153a0008c0008t0001g0152 | 2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.-9+1345A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453026 | ||||||
chr16:20453028
|
C | A | 2 | a0001c0001t0027g0153a0008c0008t0001g0152 | 2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.-9+1347C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453028 | ||||||
chr16:20453028
|
C | G | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-9+1347C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453028 | ||||||
chr16:20453029
|
G | A | 1 | a0005c0005t0001g0042 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-9+1348G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453029 | ||||||
chr16:20453092
|
C | T | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-9+1411C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453092 | ||||||
chr16:20453235
|
T | C | 1 | a0002c0002t0022g0195 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-9+1554T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453235 | ||||||
chr16:20453323
|
T | C | 1 | a0001c0018t0001g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-9+1642T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453323 | ||||||
chr16:20453420
|
C | T | 2 | a0001c0001t0001g0149a0021c0025t0005g0291 | 2 | HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-9+1739C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453420 | ||||||
chr16:20453453
|
A | C | 52 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(49): Show | 58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+1772A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453453 | ||||||
chr16:20453514
|
G | A | 6 | a0001c0001t0001g0155a0001c0001t0010g0044a0001c0001t0010g0045others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1833G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453514 | ||||||
chr16:20453577
|
T | C | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+1896T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453577 | ||||||
chr16:20453647
|
G | A | 1 | a0003c0003t0003g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9+1966G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453647 | ||||||
chr16:20453654
|
G | T | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+1973G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453654 | ||||||
chr16:20453675
|
T | C | 1 | a0003c0003t0002g0277 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+1994T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453675 | ||||||
chr16:20453740
|
G | A | 2 | a0009c0009t0006g0023a0009c0009t0006g0156 | 3 | HG02109.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-9+2059G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453740 | ||||||
chr16:20453768
|
A | G | 1 | a0004c0004t0002g0336 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-9+2087A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453768 | ||||||
chr16:20453796
|
T | G | 223 | a0001c0001t0001g0049a0001c0001t0001g0178a0002c0002t0002g0199others(220): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-9+2115T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453796 | ||||||
chr16:20453834
|
C | T | 2 | a0002c0002t0003g0266a0021c0025t0005g0291 | 2 | HG03540.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-9+2153C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453834 | ||||||
chr16:20453842
|
C | T | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2161C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453842 | ||||||
chr16:20453896
|
G | T | 7 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(4): Show | 7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2215G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453896 | ||||||
chr16:20453933
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9+2252C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453933 | ||||||
chr16:20453937
|
G | C | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+2256G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453937 | ||||||
chr16:20453992
|
C | T | 7 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(4): Show | 7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2311C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453992 | ||||||
chr16:20453995
|
C | T | 1 | a0003c0003t0002g0375 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-9+2314C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20453995 | ||||||
chr16:20454074
|
C | T | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-9+2393C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454074 | ||||||
chr16:20454075
|
A | G | 237 | a0001c0001t0001g0147a0002c0002t0002g0199a0002c0002t0002g0204others(234): Show | 266 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-9+2394A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454075 | ||||||
chr16:20454109
|
A | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+2428A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454109 | ||||||
chr16:20454126
|
G | T | 7 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(4): Show | 7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2445G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454126 | ||||||
chr16:20454129
|
C | T | 1 | a0009c0009t0001g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+2448C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454129 | ||||||
chr16:20454164
|
A | G | 6 | a0002c0002t0003g0261a0002c0002t0003g0262a0002c0002t0003g0263others(3): Show | 6 | NA18965.hp1 NA19002.hp1 NA19065.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2483A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454164 | ||||||
chr16:20454227
|
C | G | 1 | a0008c0008t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9+2546C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454227 | ||||||
chr16:20454228
|
G | A | 2 | a0002c0002t0003g0197a0002c0002t0003g0198 | 2 | HG02735.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-9+2547G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454228 | ||||||
chr16:20454272
|
G | A | 1 | a0006c0006t0002g0338 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-9+2591G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454272 | ||||||
chr16:20454360
|
T | A | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-9+2679T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454360 | ||||||
chr16:20454406
|
A | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01934.hp2 HG01943.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2725A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454406 | ||||||
chr16:20454418
|
A | T | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+2737A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454418 | ||||||
chr16:20454438
|
C | T | 93 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(90): Show | 108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-9+2757C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454438 | ||||||
chr16:20454645
|
A | G | 1 | a0005c0005t0001g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9+2964A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454645 | ||||||
chr16:20454659
|
A | G | 1 | a0009c0009t0001g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+2978A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454659 | ||||||
chr16:20454744
|
A | C | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+3063A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454744 | ||||||
chr16:20454745
|
C | A | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-9+3064C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454745 | ||||||
chr16:20454765
|
C | A | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+3084C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454765 | ||||||
chr16:20454769
|
A | C | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+3088A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454769 | ||||||
chr16:20454840
|
C | G | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-9+3159C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454840 | ||||||
chr16:20454853
|
A | C | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+3172A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454853 | ||||||
chr16:20454866
|
A | C | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+3185A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454866 | ||||||
chr16:20454900
|
G | GA | 211 | a0001c0001t0001g0024a0001c0001t0001g0179a0002c0002t0002g0199others(208): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-9+3230dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20454900 | |||||
chr16:20454900
|
GA | G | 7 | a0003c0026t0007g0170a0009c0009t0001g0167a0009c0009t0006g0023others(4): Show | 8 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3230delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20454900 | |||||
chr16:20454956
|
C | T | 7 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(4): Show | 7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3275C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20454956 | ||||||
chr16:20455006
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+3325T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455006 | ||||||
chr16:20455068
|
A | AT | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-9+3391dupT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20455068 | |||||
chr16:20455100
|
GA | G | 215 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(212): Show | 243 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.-9+3429delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20455100 | |||||
chr16:20455144
|
A | G | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+3463A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455144 | ||||||
chr16:20455152
|
A | T | 1 | a0002c0002t0009g0259 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-9+3471A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455152 | ||||||
chr16:20455165
|
T | A | 6 | a0003c0003t0002g0034a0003c0003t0002g0339a0003c0003t0002g0340others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3484T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455165 | ||||||
chr16:20455165
|
T | G | 50 | a0003c0003t0002g0037a0003c0003t0002g0272a0003c0003t0002g0282others(47): Show | 53 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+3484T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455165 | ||||||
chr16:20455178
|
C | A | 6 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(3): Show | 6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3497C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455178 | ||||||
chr16:20455198
|
C | A | 238 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(235): Show | 266 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-9+3517C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455198 | ||||||
chr16:20455251
|
A | G | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-9+3570A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455251 | ||||||
chr16:20455394
|
G | A | 52 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(49): Show | 58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+3713G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455394 | ||||||
chr16:20455418
|
A | T | 157 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(154): Show | 178 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-9+3737A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455418 | ||||||
chr16:20455486
|
C | T | 1 | a0003c0003t0002g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+3805C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455486 | ||||||
chr16:20455664
|
A | T | 6 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(3): Show | 6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3983A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455664 | ||||||
chr16:20455685
|
A | C | 1 | a0006c0006t0003g0373 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-9+4004A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455685 | ||||||
chr16:20455736
|
T | TA | 66 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0282others(63): Show | 71 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.-9+4065dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20455736 | |||||
chr16:20455823
|
C | T | 1 | a0003c0003t0005g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-9+4142C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455823 | ||||||
chr16:20455980
|
T | A | 6 | a0002c0002t0002g0199a0002c0002t0018g0200a0003c0026t0007g0170others(3): Show | 7 | HG00738.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-4127T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20455980 | ||||||
chr16:20456009
|
C | T | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-4098C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456009 | ||||||
chr16:20456247
|
A | T | 1 | a0002c0002t0003g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-8-3860A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456247 | ||||||
chr16:20456287
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-8-3820G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456287 | ||||||
chr16:20456338
|
A | G | 2 | a0003c0003t0002g0277a0003c0003t0002g0288 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-8-3769A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456338 | ||||||
chr16:20456427
|
G | C | 4 | a0003c0003t0002g0294a0004c0004t0002g0292a0004c0004t0002g0293others(1): Show | 4 | NA18988.hp2 NA18998.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3680G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456427 | ||||||
chr16:20456462
|
G | A | 222 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(219): Show | 249 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-8-3645G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456462 | ||||||
chr16:20456512
|
G | A | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-3595G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456512 | ||||||
chr16:20456560
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0179 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-8-3547A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456560 | ||||||
chr16:20456607
|
T | C | 3 | a0002c0002t0003g0201a0003c0003t0005g0175a0003c0003t0005g0176 | 3 | HG03139.hp2 HG03209.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-8-3500T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456607 | ||||||
chr16:20456664
|
T | A | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-8-3443T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456664 | ||||||
chr16:20456860
|
C | G | 1 | a0003c0003t0002g0332 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-8-3247C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456860 | ||||||
chr16:20456877
|
T | C | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-8-3230T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456877 | ||||||
chr16:20456903
|
A | G | 1 | a0004c0004t0002g0372 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-8-3204A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456903 | ||||||
chr16:20456911
|
C | CA | 62 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(59): Show | 66 | HG00673.hp2 HG00738.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8-3183dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20456911 | |||||
chr16:20456911
|
CA | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 66 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-8-3183delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20456911 | |||||
chr16:20456980
|
C | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3127C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20456980 | ||||||
chr16:20457051
|
G | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-3056G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457051 | ||||||
chr16:20457069
|
C | T | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-3038C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457069 | ||||||
chr16:20457185
|
C | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-2922C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457185 | ||||||
chr16:20457186
|
G | C | 2 | a0003c0003t0002g0277a0003c0003t0002g0288 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-8-2921G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457186 | ||||||
chr16:20457202
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-8-2905T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457202 | ||||||
chr16:20457266
|
C | T | 1 | a0005c0005t0004g0041 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-8-2841C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457266 | ||||||
chr16:20457309
|
T | G | 1 | a0002c0002t0003g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-8-2798T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457309 | ||||||
chr16:20457424
|
C | T | 1 | a0003c0003t0002g0370 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-2683C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457424 | ||||||
chr16:20457486
|
C | T | 157 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(154): Show | 178 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-8-2621C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457486 | ||||||
chr16:20457509
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-8-2598C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457509 | ||||||
chr16:20457552
|
A | T | 2 | a0002c0002t0003g0197a0002c0002t0003g0198 | 2 | HG02735.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-8-2555A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457552 | ||||||
chr16:20457566
|
A | C | 2 | a0002c0002t0015g0256a0003c0003t0002g0342 | 2 | HG02818.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-8-2541A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457566 | ||||||
chr16:20457626
|
T | C | 46 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0339others(43): Show | 50 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-8-2481T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457626 | ||||||
chr16:20457666
|
T | C | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-2441T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457666 | ||||||
chr16:20457690
|
T | C | 1 | a0002c0002t0002g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-8-2417T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457690 | ||||||
chr16:20457702
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-2405C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457702 | ||||||
chr16:20457882
|
G | C | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-8-2225G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457882 | ||||||
chr16:20457898
|
A | G | 1 | a0003c0003t0002g0331 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-8-2209A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20457898 | ||||||
chr16:20458025
|
A | G | 1 | a0002c0002t0002g0255 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-8-2082A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458025 | ||||||
chr16:20458104
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | HG01891.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-2003C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458104 | ||||||
chr16:20458196
|
G | A | 4 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0012g0171others(1): Show | 4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1911G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458196 | ||||||
chr16:20458283
|
T | G | 9 | a0003c0003t0002g0277a0003c0003t0002g0288a0003c0003t0005g0030others(6): Show | 11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1824T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458283 | ||||||
chr16:20458445
|
C | CA | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-8-1662_-8-1661ins others(1): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458445 | ||||||
chr16:20458485
|
T | C | 52 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(49): Show | 58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-8-1622T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458485 | ||||||
chr16:20458661
|
A | T | 2 | a0005c0005t0016g0137a0005c0005t0016g0138 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.-8-1446A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458661 | ||||||
chr16:20458694
|
CTA | C | 7 | a0006c0006t0002g0270a0006c0006t0002g0364a0006c0006t0002g0365others(4): Show | 7 | NA18956.hp1 NA18968.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1403_-8-1402del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458694 | |||||
chr16:20458723
|
G | A | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1384G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458723 | ||||||
chr16:20458809
|
A | T | 1 | a0009c0009t0006g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-1298A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458809 | ||||||
chr16:20458840
|
G | T | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-8-1267G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458840 | ||||||
chr16:20458892
|
T | TTATATAT others(17): Show |
1 | a0005c0005t0001g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8-1203_-8-1180dup others(24): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458892 | |||||
chr16:20458896
|
A | ATATATAT others(3): Show |
1 | a0003c0003t0005g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-1204_-8-1203ins others(10): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458896 | |||||
chr16:20458897
|
TATATATG others(1): Show |
T | 5 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1196del others(8): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458897 | |||||
chr16:20458897
|
TATATATG others(29): Show |
T | 160 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(157): Show | 181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1168del others(36): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458897 | |||||
chr16:20458899
|
TATATGCA others(27): Show |
T | 2 | a0003c0003t0003g0254a0004c0004t0013g0379 | 2 | HG04199.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1203_-8-1170del others(34): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458899 | |||||
chr16:20458901
|
TATGC | T | 8 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1200del others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458901 | |||||
chr16:20458903
|
TGCATATA others(2): Show |
T | 10 | a0003c0003t0002g0033a0004c0004t0002g0295a0004c0004t0002g0322others(7): Show | 11 | HG00621.hp1 HG02148.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1195del others(9): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458903 | ||||||
chr16:20458903
|
TGCATATA others(4): Show |
T | 38 | a0003c0003t0002g0294a0003c0003t0002g0305a0003c0003t0002g0306others(35): Show | 43 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8-1203_-8-1193del others(11): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458903 | ||||||
chr16:20458903
|
TGCATATA others(6): Show |
T | 2 | a0004c0004t0002g0297a0004c0004t0002g0298 | 2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1203_-8-1191del others(13): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458903 | ||||||
chr16:20458904
|
G | A | 3 | a0003c0003t0005g0175a0003c0003t0005g0176a0008c0008t0001g0146 | 3 | HG02055.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-1203G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458904 | ||||||
chr16:20458904
|
G | GTATATAT others(23): Show |
1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-1203_-8-1202ins others(30): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458904 | ||||||
chr16:20458905
|
C | CAT | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(22): Show | 37 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.-8-1176_-8-1175dup others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | CATAT | 3 | a0001c0001t0001g0192a0001c0001t0006g0090a0010c0012t0001g0052 | 3 | HG01433.hp1 HG02055.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-8-1178_-8-1175dup others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | CATATAT | 4 | a0001c0001t0001g0039a0001c0001t0001g0091a0001c0001t0027g0153others(1): Show | 4 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1180_-8-1175dup others(6): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | CATATATA others(1): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0093others(3): Show | 8 | HG01168.hp2 HG01169.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1182_-8-1175dup others(8): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0096 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8-1184_-8-1175dup others(10): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | CATATATA others(5): Show |
4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG01993.hp1 HG02602.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1186_-8-1175dup others(12): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | CATATATA others(9): Show |
2 | a0001c0001t0001g0168a0001c0001t0024g0169 | 2 | NA18955.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-8-1190_-8-1175dup others(16): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458905
|
C | T | 8 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(5): Show | 8 | HG02055.hp2 HG03139.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-1202C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458905 | ||||||
chr16:20458905
|
CAT | C | 21 | a0001c0001t0001g0066a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 22 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-1176_-8-1175del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458905 | |||||
chr16:20458906
|
A | G | 1 | a0008c0008t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8-1201A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458906 | ||||||
chr16:20458907
|
T | C | 1 | a0008c0008t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8-1200T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458907 | ||||||
chr16:20458909
|
T | TATATATA others(3): Show |
2 | a0003c0003t0012g0171a0003c0003t0012g0172 | 2 | HG03831.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-8-1189_-8-1188ins others(10): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20458909 | |||||
chr16:20458910
|
A | G | 8 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1197A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458910 | ||||||
chr16:20458911
|
T | A | 2 | a0004c0004t0002g0329a0004c0004t0002g0330 | 2 | HG01978.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-1196T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458911 | ||||||
chr16:20458912
|
A | G | 2 | a0004c0004t0002g0329a0004c0004t0002g0330 | 2 | HG01978.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-1195A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458912 | ||||||
chr16:20458913
|
T | A | 10 | a0003c0003t0002g0033a0004c0004t0002g0295a0004c0004t0002g0322others(7): Show | 11 | HG00621.hp1 HG02148.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1194T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458913 | ||||||
chr16:20458914
|
A | G | 18 | a0003c0003t0002g0033a0004c0004t0002g0295a0004c0004t0002g0322others(15): Show | 20 | HG00621.hp1 HG01978.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-1193A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458914 | ||||||
chr16:20458915
|
T | A | 38 | a0003c0003t0002g0294a0003c0003t0002g0305a0003c0003t0002g0306others(35): Show | 43 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8-1192T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458915 | ||||||
chr16:20458916
|
A | G | 48 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(45): Show | 54 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-1191A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458916 | ||||||
chr16:20458917
|
T | A | 2 | a0004c0004t0002g0297a0004c0004t0002g0298 | 2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1190T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458917 | ||||||
chr16:20458918
|
A | G | 40 | a0003c0003t0002g0294a0003c0003t0002g0305a0003c0003t0002g0306others(37): Show | 45 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-1189A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458918 | ||||||
chr16:20458920
|
A | G | 2 | a0004c0004t0002g0297a0004c0004t0002g0298 | 2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1187A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458920 | ||||||
chr16:20458921
|
T | C | 8 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-1186T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458921 | ||||||
chr16:20458925
|
T | C | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1182T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458925 | ||||||
chr16:20458931
|
T | C | 1 | a0005c0005t0004g0130 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-8-1176T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458931 | ||||||
chr16:20458932
|
A | ATG | 3 | a0007c0007t0001g0101a0007c0007t0001g0102a0007c0007t0001g0103 | 3 | HG01934.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-1175_-8-1174ins others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458932 | ||||||
chr16:20458932
|
A | G | 2 | a0007c0007t0023g0104a0007c0007t0028g0105 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-1175A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458932 | ||||||
chr16:20458933
|
C | T | 73 | a0003c0003t0002g0033a0003c0003t0002g0173a0003c0003t0002g0174others(70): Show | 80 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-8-1174C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458933 | ||||||
chr16:20458935
|
T | C | 2 | a0001c0001t0026g0061a0008c0008t0001g0015 | 3 | HG01099.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8-1172T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458935 | ||||||
chr16:20458986
|
G | T | 2 | a0004c0004t0002g0297a0004c0004t0002g0298 | 2 | NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-8-1121G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20458986 | ||||||
chr16:20459141
|
T | C | 1 | a0004c0004t0002g0299 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-8-966T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459141 | ||||||
chr16:20459163
|
G | C | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-944G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459163 | ||||||
chr16:20459231
|
T | A | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-876T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459231 | ||||||
chr16:20459322
|
T | A | 1 | a0004c0004t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-8-785T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459322 | ||||||
chr16:20459402
|
T | A | 2 | a0006c0006t0002g0343a0006c0006t0019g0344 | 2 | NA18978.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-8-705T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459402 | ||||||
chr16:20459403
|
T | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-704T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459403 | ||||||
chr16:20459406
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-8-701A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459406 | ||||||
chr16:20459479
|
A | G | 1 | a0004c0004t0002g0321 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-8-628A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459479 | ||||||
chr16:20459768
|
T | C | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-8-339T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459768 | ||||||
chr16:20459853
|
G | A | 1 | a0003c0003t0005g0285 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-254G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459853 | ||||||
chr16:20459855
|
G | A | 82 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(79): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-8-252G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459855 | ||||||
chr16:20459870
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.-8-237T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459870 | ||||||
chr16:20459887
|
G | T | 9 | a0003c0003t0002g0277a0003c0003t0002g0288a0003c0003t0005g0030others(6): Show | 11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-220G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459887 | ||||||
chr16:20459898
|
G | C | 1 | a0010c0012t0001g0014 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-8-209G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459898 | ||||||
chr16:20459963
|
T | A | 1 | a0004c0004t0002g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-144T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459963 | ||||||
chr16:20459984
|
C | A | 1 | a0007c0007t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-123C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20459984 | ||||||
chr16:20460042
|
T | C | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-8-65T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460042 | ||||||
chr16:20460057
|
G | C | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-50G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460057 | ||||||
chr16:20460059
|
G | A | 2 | a0001c0001t0010g0044a0001c0001t0010g0045 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-8-48G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460059 | ||||||
chr16:20460105
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-8-2A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 1/13 | chr16 | 20460105 | ||||||
chr16:20460304
|
A | C | 1 | a0004c0004t0002g0320 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.177+13A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460304 | ||||||
chr16:20460412
|
G | A | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.177+121G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460412 | ||||||
chr16:20460424
|
G | A | 3 | a0005c0005t0016g0137a0005c0005t0016g0138a0005c0005t0032g0132 | 3 | HG00099.hp1 HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.177+133G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460424 | ||||||
chr16:20460543
|
A | G | 1 | a0005c0005t0004g0067 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.177+252A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460543 | ||||||
chr16:20460609
|
G | A | 1 | a0002c0002t0003g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.177+318G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460609 | ||||||
chr16:20460663
|
C | T | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.177+372C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460663 | ||||||
chr16:20460728
|
A | T | 1 | a0005c0005t0030g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.177+437A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460728 | ||||||
chr16:20460812
|
A | G | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.177+521A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460812 | ||||||
chr16:20460813
|
C | T | 1 | a0003c0003t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.177+522C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20460813 | ||||||
chr16:20461154
|
G | A | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.177+863G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461154 | ||||||
chr16:20461260
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.177+969C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461260 | ||||||
chr16:20461430
|
A | G | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+1139A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461430 | ||||||
chr16:20461436
|
C | T | 1 | a0006c0006t0002g0363 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.177+1145C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461436 | ||||||
chr16:20461486
|
A | C | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+1195A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461486 | ||||||
chr16:20461488
|
T | C | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+1197T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461488 | ||||||
chr16:20461491
|
C | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+1200C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461491 | ||||||
chr16:20461539
|
G | A | 1 | a0006c0006t0002g0363 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.177+1248G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461539 | ||||||
chr16:20461541
|
A | G | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.177+1250A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461541 | ||||||
chr16:20461723
|
A | G | 1 | a0007c0007t0001g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+1432A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461723 | ||||||
chr16:20461951
|
C | G | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+1660C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461951 | ||||||
chr16:20461954
|
A | G | 237 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(234): Show | 265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.177+1663A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20461954 | ||||||
chr16:20462137
|
A | G | 2 | a0004c0004t0002g0317a0004c0004t0002g0318 | 2 | HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.177+1846A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462137 | ||||||
chr16:20462140
|
G | C | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+1849G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462140 | ||||||
chr16:20462156
|
G | A | 4 | a0001c0001t0001g0069a0003c0003t0007g0011a0003c0003t0007g0249others(1): Show | 6 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+1865G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462156 | ||||||
chr16:20462272
|
A | G | 51 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(48): Show | 57 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.177+1981A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462272 | ||||||
chr16:20462274
|
A | G | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.177+1983A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462274 | ||||||
chr16:20462442
|
C | T | 1 | a0002c0002t0003g0201 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.177+2151C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462442 | ||||||
chr16:20462470
|
T | G | 1 | a0002c0002t0003g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.177+2179T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462470 | ||||||
chr16:20462471
|
C | T | 1 | a0002c0002t0003g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.177+2180C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462471 | ||||||
chr16:20462581
|
G | A | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.177+2290G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462581 | ||||||
chr16:20462637
|
C | A | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.177+2346C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462637 | ||||||
chr16:20462713
|
A | G | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+2422A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462713 | ||||||
chr16:20462796
|
C | G | 2 | a0003c0003t0002g0272a0003c0003t0007g0271 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.177+2505C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462796 | ||||||
chr16:20462821
|
T | A | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.177+2530T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462821 | ||||||
chr16:20462828
|
C | CA | 8 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+2545dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20462828 | |||||
chr16:20462982
|
C | CA | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0010g0044others(1): Show | 4 | HG01175.hp1 HG02897.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-2528dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20462982 | |||||
chr16:20462998
|
A | C | 238 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(235): Show | 266 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.178-2519A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462998 | ||||||
chr16:20462998
|
A | T | 1 | a0005c0005t0001g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.178-2519A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20462998 | ||||||
chr16:20463008
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.178-2509C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463008 | ||||||
chr16:20463031
|
A | G | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2486A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463031 | ||||||
chr16:20463061
|
A | T | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178-2456A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463061 | ||||||
chr16:20463098
|
G | T | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.178-2419G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463098 | ||||||
chr16:20463109
|
A | T | 1 | a0003c0010t0006g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-2408A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463109 | ||||||
chr16:20463115
|
C | T | 341 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(338): Show | 388 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(385): Show |
intron_variant | MODIFIER | c.178-2402C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463115 | ||||||
chr16:20463125
|
A | G | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.178-2392A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463125 | ||||||
chr16:20463137
|
C | T | 1 | a0002c0002t0003g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.178-2380C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463137 | ||||||
chr16:20463138
|
G | A | 1 | a0002c0002t0003g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.178-2379G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463138 | ||||||
chr16:20463169
|
C | T | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.178-2348C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463169 | ||||||
chr16:20463181
|
T | C | 6 | a0002c0002t0003g0208a0002c0002t0008g0009a0002c0002t0008g0193others(3): Show | 8 | NA18940.hp2 NA18948.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-2336T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463181 | ||||||
chr16:20463190
|
C | T | 1 | a0002c0002t0003g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.178-2327C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463190 | ||||||
chr16:20463206
|
A | C | 2 | a0007c0007t0001g0082a0007c0007t0001g0083 | 2 | HG01496.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.178-2311A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463206 | ||||||
chr16:20463231
|
T | C | 5 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(2): Show | 7 | HG01884.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2286T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463231 | ||||||
chr16:20463264
|
A | C | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-2253A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463264 | ||||||
chr16:20463270
|
A | G | 2 | a0003c0003t0002g0283a0003c0003t0002g0284 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.178-2247A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463270 | ||||||
chr16:20463345
|
G | T | 1 | a0002c0002t0003g0247 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.178-2172G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463345 | ||||||
chr16:20463360
|
T | C | 237 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(234): Show | 265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.178-2157T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463360 | ||||||
chr16:20463462
|
C | A | 1 | a0002c0002t0003g0211 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.178-2055C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463462 | ||||||
chr16:20463479
|
G | A | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2038G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463479 | ||||||
chr16:20463647
|
A | T | 6 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(3): Show | 6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1870A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463647 | ||||||
chr16:20463697
|
G | A | 1 | a0018c0029t0001g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.178-1820G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463697 | ||||||
chr16:20463728
|
A | G | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178-1789A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463728 | ||||||
chr16:20463767
|
G | A | 1 | a0008c0008t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.178-1750G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463767 | ||||||
chr16:20463885
|
T | C | 1 | a0004c0004t0002g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178-1632T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463885 | ||||||
chr16:20463906
|
C | T | 1 | a0006c0006t0002g0362 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.178-1611C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463906 | ||||||
chr16:20463932
|
C | T | 91 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(88): Show | 106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.178-1585C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463932 | ||||||
chr16:20463956
|
C | G | 227 | a0001c0001t0001g0155a0001c0001t0010g0044a0001c0001t0010g0045others(224): Show | 254 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.178-1561C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463956 | ||||||
chr16:20463983
|
C | T | 1 | a0002c0002t0003g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178-1534C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20463983 | ||||||
chr16:20464091
|
G | C | 5 | a0001c0001t0027g0153a0003c0003t0005g0175a0003c0003t0005g0176others(2): Show | 5 | HG00558.hp1 HG00609.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1426G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464091 | ||||||
chr16:20464120
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0088a0001c0001t0001g0100 | 4 | HG01168.hp2 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-1397A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464120 | ||||||
chr16:20464147
|
G | T | 1 | a0008c0008t0001g0038 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.178-1370G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464147 | ||||||
chr16:20464201
|
G | A | 1 | a0006c0006t0002g0364 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178-1316G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464201 | ||||||
chr16:20464228
|
G | T | 52 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(49): Show | 58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.178-1289G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464228 | ||||||
chr16:20464245
|
T | A | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.178-1272T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464245 | ||||||
chr16:20464357
|
C | T | 52 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(49): Show | 58 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.178-1160C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464357 | ||||||
chr16:20464412
|
T | C | 237 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(234): Show | 265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.178-1105T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464412 | ||||||
chr16:20464436
|
C | T | 1 | a0005c0005t0029g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.178-1081C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464436 | ||||||
chr16:20464499
|
T | C | 1 | a0003c0003t0002g0250 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-1018T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464499 | ||||||
chr16:20464562
|
ATCTTATG others(449): Show |
A | 1 | a0004c0004t0002g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-953_178-498del | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20464562 | |||||
chr16:20464607
|
C | T | 2 | a0002c0002t0002g0199a0002c0002t0018g0200 | 2 | HG00738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.178-910C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464607 | ||||||
chr16:20464622
|
C | G | 1 | a0006c0006t0002g0361 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.178-895C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464622 | ||||||
chr16:20464735
|
A | T | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-782A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464735 | ||||||
chr16:20464749
|
G | A | 2 | a0002c0002t0003g0197a0002c0002t0003g0198 | 2 | HG02735.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.178-768G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464749 | ||||||
chr16:20464796
|
G | A | 1 | a0004c0004t0002g0322 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.178-721G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464796 | ||||||
chr16:20464811
|
G | A | 1 | a0003c0003t0002g0345 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178-706G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464811 | ||||||
chr16:20464988
|
A | T | 1 | a0003c0003t0003g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.178-529A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20464988 | ||||||
chr16:20465016
|
G | T | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.178-501G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465016 | ||||||
chr16:20465019
|
T | G | 1 | a0004c0004t0002g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-498T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465019 | ||||||
chr16:20465020
|
T | G | 1 | a0004c0004t0002g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-497T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465020 | ||||||
chr16:20465021
|
T | G | 1 | a0004c0004t0002g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-496T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465021 | ||||||
chr16:20465155
|
A | G | 215 | a0001c0001t0006g0090a0002c0002t0002g0199a0002c0002t0002g0204others(212): Show | 242 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.178-362A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465155 | ||||||
chr16:20465164
|
C | T | 1 | a0003c0003t0005g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178-353C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465164 | ||||||
chr16:20465250
|
T | C | 1 | a0003c0003t0002g0339 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.178-267T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465250 | ||||||
chr16:20465364
|
G | C | 92 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(89): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.178-153G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465364 | ||||||
chr16:20465372
|
A | G | 92 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(89): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.178-145A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465372 | ||||||
chr16:20465373
|
A | G | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.178-144A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465373 | ||||||
chr16:20465408
|
G | A | 1 | a0005c0005t0001g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.178-109G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465408 | ||||||
chr16:20465469
|
T | A | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.178-48T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465469 | ||||||
chr16:20465491
|
G | A | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.178-26G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465491 | ||||||
chr16:20465502
|
C | T | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.178-15C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465502 | ||||||
chr16:20465514
|
C | T | 1 | a0002c0002t0003g0245 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.178-3C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 2/13 | chr16 | 20465514 | ||||||
chr16:20465779
|
G | A | 1 | a0005c0005t0004g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.388+52G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465779 | ||||||
chr16:20465781
|
T | G | 1 | a0004c0004t0002g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.388+54T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465781 | ||||||
chr16:20465821
|
T | G | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+94T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465821 | ||||||
chr16:20465841
|
G | C | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.388+114G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465841 | ||||||
chr16:20465843
|
A | C | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.388+116A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465843 | ||||||
chr16:20465860
|
A | T | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+133A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465860 | ||||||
chr16:20465868
|
A | G | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+141A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20465868 | ||||||
chr16:20466023
|
T | G | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+296T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466023 | ||||||
chr16:20466052
|
A | C | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+325A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466052 | ||||||
chr16:20466065
|
C | T | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+338C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466065 | ||||||
chr16:20466097
|
A | C | 8 | a0002c0002t0002g0199a0002c0002t0003g0027a0002c0002t0003g0242others(5): Show | 9 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+370A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466097 | ||||||
chr16:20466134
|
G | GCTATGCC others(12): Show |
8 | a0002c0002t0002g0199a0002c0002t0003g0027a0002c0002t0003g0242others(5): Show | 9 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+407_388+408ins others(19): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466134 | ||||||
chr16:20466152
|
G | T | 346 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(343): Show | 393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.388+425G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466152 | ||||||
chr16:20466160
|
A | G | 8 | a0002c0002t0002g0199a0002c0002t0003g0027a0002c0002t0003g0242others(5): Show | 9 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+433A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466160 | ||||||
chr16:20466176
|
T | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+449T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466176 | ||||||
chr16:20466186
|
A | G | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+459A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466186 | ||||||
chr16:20466244
|
AG | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0069 | 4 | HG00735.hp2 HG01109.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+518delG | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466244 | ||||||
chr16:20466267
|
G | A | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+540G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466267 | ||||||
chr16:20466268
|
A | G | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+541A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466268 | ||||||
chr16:20466410
|
A | C | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+683A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466410 | ||||||
chr16:20466475
|
T | C | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.388+748T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466475 | ||||||
chr16:20466476
|
G | A | 218 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(215): Show | 245 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.388+749G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466476 | ||||||
chr16:20466538
|
A | G | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.388+811A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466538 | ||||||
chr16:20466589
|
T | A | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.388+862T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466589 | ||||||
chr16:20466697
|
A | G | 1 | a0013c0021t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.388+970A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466697 | ||||||
chr16:20466789
|
A | T | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388+1062A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466789 | ||||||
chr16:20466820
|
A | C | 2 | a0009c0009t0006g0154a0009c0009t0006g0165 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.388+1093A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466820 | ||||||
chr16:20466837
|
T | A | 1 | a0006c0006t0002g0362 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.388+1110T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466837 | ||||||
chr16:20466938
|
G | A | 1 | a0003c0003t0003g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.388+1211G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20466938 | ||||||
chr16:20467008
|
C | G | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+1281C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467008 | ||||||
chr16:20467109
|
A | G | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.388+1382A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467109 | ||||||
chr16:20467114
|
T | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(14): Show | 21 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+1387T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467114 | ||||||
chr16:20467124
|
G | T | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+1397G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467124 | ||||||
chr16:20467162
|
A | G | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+1435A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467162 | ||||||
chr16:20467260
|
C | T | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.388+1533C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467260 | ||||||
chr16:20467280
|
T | A | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.388+1553T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467280 | ||||||
chr16:20467331
|
GATTGAGT others(20): Show |
G | 46 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0339others(43): Show | 50 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.388+1633_388+1659d others(29): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 20467331 | |||||
chr16:20467402
|
C | A | 295 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0017others(292): Show | 329 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.388+1675C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467402 | ||||||
chr16:20467410
|
T | C | 1 | a0016c0028t0001g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.388+1683T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467410 | ||||||
chr16:20467494
|
C | T | 7 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(4): Show | 7 | HG03139.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+1767C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467494 | ||||||
chr16:20467561
|
G | T | 2 | a0003c0003t0002g0272a0003c0003t0007g0271 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.388+1834G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467561 | ||||||
chr16:20467613
|
G | T | 2 | a0003c0003t0012g0171a0003c0003t0012g0172 | 2 | HG03831.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.388+1886G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467613 | ||||||
chr16:20467648
|
C | T | 4 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0012g0171others(1): Show | 4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.389-1864C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20467648 | ||||||
chr16:20468021
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.389-1491A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468021 | ||||||
chr16:20468028
|
C | T | 2 | a0003c0003t0002g0277a0003c0003t0002g0288 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.389-1484C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468028 | ||||||
chr16:20468067
|
C | T | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.389-1445C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468067 | ||||||
chr16:20468286
|
G | T | 1 | a0006c0016t0002g0360 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.389-1226G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468286 | ||||||
chr16:20468418
|
G | T | 1 | a0006c0006t0002g0369 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.389-1094G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468418 | ||||||
chr16:20468462
|
C | A | 1 | a0004c0004t0002g0323 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.389-1050C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468462 | ||||||
chr16:20468691
|
T | A | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.389-821T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468691 | ||||||
chr16:20468721
|
C | T | 9 | a0003c0003t0002g0277a0003c0003t0002g0288a0003c0003t0005g0030others(6): Show | 11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-791C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468721 | ||||||
chr16:20468978
|
A | G | 1 | a0003c0003t0005g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.389-534A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20468978 | ||||||
chr16:20469024
|
G | C | 56 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0272others(53): Show | 60 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.389-488G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469024 | ||||||
chr16:20469122
|
A | T | 148 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(145): Show | 167 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.389-390A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469122 | ||||||
chr16:20469205
|
AT | A | 57 | a0001c0001t0001g0115a0003c0003t0002g0034a0003c0003t0002g0037others(54): Show | 61 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.389-299delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 20469205 | |||||
chr16:20469287
|
C | A | 3 | a0001c0001t0001g0066a0001c0017t0001g0064a0001c0017t0001g0065 | 3 | HG02486.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.389-225C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469287 | ||||||
chr16:20469357
|
T | A | 162 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(159): Show | 183 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.389-155T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469357 | ||||||
chr16:20469496
|
T | C | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.389-16T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 3/13 | chr16 | 20469496 | ||||||
chr16:20469786
|
C | T | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+67C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469786 | ||||||
chr16:20469870
|
GTA | G | 136 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(133): Show | 158 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(155): Show |
intron_variant | MODIFIER | c.596+153_596+154del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469870 | |||||
chr16:20469870
|
GTAT | G | 50 | a0002c0002t0003g0197a0003c0003t0002g0033a0003c0003t0002g0272others(47): Show | 56 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.596+153_596+155del others(3): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469870 | |||||
chr16:20469871
|
TA | T | 33 | a0002c0002t0003g0010a0002c0002t0003g0177a0002c0002t0003g0205others(30): Show | 33 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.596+153delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469871 | ||||||
chr16:20469872
|
A | AT | 8 | a0001c0001t0001g0058a0001c0001t0001g0129a0001c0001t0004g0021others(5): Show | 9 | HG00621.hp2 HG01261.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+177dupT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469872 | |||||
chr16:20469872
|
A | T | 15 | a0002c0002t0008g0210a0003c0003t0002g0282a0003c0003t0002g0284others(12): Show | 15 | HG00741.hp1 HG01361.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.596+153A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469872 | ||||||
chr16:20469872
|
AT | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 51 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.596+177delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469872 | |||||
chr16:20469872
|
ATT | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0086a0001c0001t0001g0088others(11): Show | 15 | HG01168.hp2 HG01169.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.596+176_596+177del others(2): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20469872 | |||||
chr16:20469883
|
T | G | 1 | a0006c0006t0002g0364 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.596+164T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469883 | ||||||
chr16:20469884
|
T | G | 44 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0339others(41): Show | 48 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.596+165T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469884 | ||||||
chr16:20469885
|
T | G | 2 | a0006c0006t0002g0347a0006c0006t0009g0346 | 2 | NA18994.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.596+166T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20469885 | ||||||
chr16:20470077
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG00738.hp2 HG01261.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.596+358C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470077 | ||||||
chr16:20470093
|
C | G | 222 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(219): Show | 249 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.596+374C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470093 | ||||||
chr16:20470150
|
T | C | 1 | a0008c0008t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470150 | ||||||
chr16:20470175
|
A | G | 1 | a0008c0008t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+456A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470175 | ||||||
chr16:20470180
|
A | G | 1 | a0003c0003t0003g0252 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.596+461A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470180 | ||||||
chr16:20470248
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.596+529C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470248 | ||||||
chr16:20470294
|
C | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0053others(4): Show | 10 | HG00099.hp2 HG00735.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.596+575C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470294 | ||||||
chr16:20470334
|
T | C | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.596+615T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470334 | ||||||
chr16:20470350
|
A | T | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.596+631A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470350 | ||||||
chr16:20470413
|
T | C | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-660T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470413 | ||||||
chr16:20470555
|
C | T | 2 | a0003c0003t0002g0272a0003c0003t0007g0271 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.597-518C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470555 | ||||||
chr16:20470630
|
T | A | 1 | a0004c0004t0002g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597-443T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470630 | ||||||
chr16:20470639
|
A | G | 2 | a0001c0001t0001g0186a0003c0003t0002g0339 | 2 | HG02135.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.597-434A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470639 | ||||||
chr16:20470664
|
T | C | 1 | a0005c0005t0001g0022 | 2 | HG01175.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.597-409T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470664 | ||||||
chr16:20470685
|
G | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.597-388G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470685 | ||||||
chr16:20470706
|
A | G | 4 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0012g0171others(1): Show | 4 | HG03831.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-367A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470706 | ||||||
chr16:20470744
|
T | C | 8 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(5): Show | 8 | HG00423.hp2 HG00544.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-329T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470744 | ||||||
chr16:20470831
|
C | G | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-242C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20470831 | ||||||
chr16:20471002
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.597-71A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20471002 | ||||||
chr16:20471046
|
A | G | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.597-27A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 4/13 | chr16 | 20471046 | ||||||
chr16:20471301
|
G | T | 237 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(234): Show | 265 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.740+85G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471301 | ||||||
chr16:20471367
|
CT | C | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+155delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 20471367 | |||||
chr16:20471416
|
C | A | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.741-120C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471416 | ||||||
chr16:20471429
|
A | G | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.741-107A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471429 | ||||||
chr16:20471440
|
C | T | 1 | a0005c0005t0001g0144 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.741-96C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471440 | ||||||
chr16:20471452
|
C | T | 6 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0175others(3): Show | 6 | HG03139.hp2 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-84C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471452 | ||||||
chr16:20471468
|
C | A | 53 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(50): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.741-68C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471468 | ||||||
chr16:20471482
|
G | A | 3 | a0002c0002t0003g0261a0002c0002t0003g0264a0002c0002t0003g0265 | 3 | NA18965.hp1 NA19002.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.741-54G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 5/13 | chr16 | 20471482 | ||||||
chr16:20471701
|
T | A | 4 | a0003c0003t0003g0303a0004c0004t0002g0302a0004c0004t0002g0313others(1): Show | 4 | HG02148.hp1 NA18960.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+12T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471701 | ||||||
chr16:20471754
|
A | T | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.894+65A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471754 | ||||||
chr16:20471778
|
A | G | 9 | a0003c0003t0002g0277a0003c0003t0002g0288a0003c0003t0005g0030others(6): Show | 11 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.894+89A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471778 | ||||||
chr16:20471966
|
G | C | 1 | a0001c0018t0001g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.894+277G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20471966 | ||||||
chr16:20472007
|
G | A | 1 | a0011c0011t0005g0275 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.894+318G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472007 | ||||||
chr16:20472041
|
G | A | 2 | a0003c0003t0002g0283a0003c0003t0002g0284 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.894+352G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472041 | ||||||
chr16:20472407
|
T | C | 8 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+718T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472407 | ||||||
chr16:20472467
|
C | T | 2 | a0001c0001t0027g0153a0008c0008t0001g0152 | 2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.894+778C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472467 | ||||||
chr16:20472639
|
G | A | 214 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(211): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.894+950G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472639 | ||||||
chr16:20472640
|
C | T | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+951C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472640 | ||||||
chr16:20472663
|
A | C | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+974A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472663 | ||||||
chr16:20472667
|
A | G | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+978A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472667 | ||||||
chr16:20472673
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.894+984T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472673 | ||||||
chr16:20472675
|
C | T | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+986C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472675 | ||||||
chr16:20472706
|
TG | T | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1019delG | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 20472706 | |||||
chr16:20472709
|
A | C | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1020A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472709 | ||||||
chr16:20472726
|
G | A | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1037G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472726 | ||||||
chr16:20472728
|
C | A | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1039C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472728 | ||||||
chr16:20472730
|
A | C | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1041A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472730 | ||||||
chr16:20472738
|
G | A | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1049G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472738 | ||||||
chr16:20472748
|
G | T | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.894+1059G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472748 | ||||||
chr16:20472794
|
C | T | 3 | a0002c0002t0003g0026a0002c0002t0003g0211a0002c0002t0003g0247 | 4 | NA18962.hp2 NA19002.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+1105C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472794 | ||||||
chr16:20472848
|
A | G | 1 | a0003c0003t0002g0339 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.894+1159A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472848 | ||||||
chr16:20472849
|
T | C | 2 | a0003c0003t0002g0283a0003c0003t0002g0284 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.894+1160T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472849 | ||||||
chr16:20472898
|
T | C | 1 | a0004c0004t0002g0313 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.894+1209T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20472898 | ||||||
chr16:20473068
|
C | T | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.894+1379C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473068 | ||||||
chr16:20473322
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.894+1633T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473322 | ||||||
chr16:20473495
|
G | A | 1 | a0002c0002t0003g0213 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.894+1806G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473495 | ||||||
chr16:20473548
|
G | T | 161 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(158): Show | 182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.895-1814G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473548 | ||||||
chr16:20473665
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.895-1697A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473665 | ||||||
chr16:20473678
|
G | A | 1 | a0004c0004t0002g0304 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.895-1684G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473678 | ||||||
chr16:20473755
|
T | C | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.895-1607T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473755 | ||||||
chr16:20473818
|
A | T | 2 | a0002c0002t0003g0240a0012c0013t0002g0236 | 2 | HG00408.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.895-1544A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473818 | ||||||
chr16:20473849
|
G | A | 238 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(235): Show | 266 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.895-1513G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473849 | ||||||
chr16:20473857
|
T | A | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.895-1505T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473857 | ||||||
chr16:20473895
|
A | G | 10 | a0002c0002t0002g0199a0002c0002t0002g0234a0002c0002t0003g0027others(7): Show | 11 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.895-1467A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473895 | ||||||
chr16:20473914
|
C | T | 244 | a0001c0001t0001g0155a0001c0001t0010g0044a0001c0001t0010g0045others(241): Show | 272 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.895-1448C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473914 | ||||||
chr16:20473919
|
A | C | 244 | a0001c0001t0001g0155a0001c0001t0010g0044a0001c0001t0010g0045others(241): Show | 272 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.895-1443A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473919 | ||||||
chr16:20473931
|
T | C | 244 | a0001c0001t0001g0155a0001c0001t0010g0044a0001c0001t0010g0045others(241): Show | 272 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.895-1431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473931 | ||||||
chr16:20473935
|
G | A | 161 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(158): Show | 182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.895-1427G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20473935 | ||||||
chr16:20474064
|
A | G | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.895-1298A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474064 | ||||||
chr16:20474092
|
T | C | 1 | a0004c0004t0002g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.895-1270T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474092 | ||||||
chr16:20474144
|
C | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.895-1218C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474144 | ||||||
chr16:20474158
|
A | C | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.895-1204A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474158 | ||||||
chr16:20474225
|
T | C | 1 | a0006c0006t0002g0363 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.895-1137T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474225 | ||||||
chr16:20474266
|
T | C | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1096T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474266 | ||||||
chr16:20474282
|
G | A | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(4): Show | 7 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1080G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474282 | ||||||
chr16:20474318
|
G | A | 2 | a0003c0003t0002g0272a0003c0003t0007g0271 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.895-1044G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474318 | ||||||
chr16:20474324
|
T | A | 1 | a0004c0014t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.895-1038T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474324 | ||||||
chr16:20474341
|
C | A | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.895-1021C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474341 | ||||||
chr16:20474377
|
T | C | 3 | a0005c0005t0016g0137a0005c0005t0016g0138a0005c0005t0032g0132 | 3 | HG00099.hp1 HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.895-985T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474377 | ||||||
chr16:20474473
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0024others(6): Show | 16 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.895-889C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474473 | ||||||
chr16:20474655
|
C | T | 4 | a0011c0011t0005g0274a0011c0011t0005g0275a0011c0011t0005g0276others(1): Show | 4 | HG02145.hp2 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-707C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474655 | ||||||
chr16:20474718
|
C | G | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.895-644C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474718 | ||||||
chr16:20474893
|
A | G | 2 | a0004c0004t0002g0304a0004c0004t0002g0328 | 2 | HG00621.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.895-469A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474893 | ||||||
chr16:20474917
|
T | C | 2 | a0002c0002t0003g0242a0002c0002t0003g0243 | 2 | HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.895-445T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20474917 | ||||||
chr16:20475043
|
G | A | 53 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(50): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.895-319G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475043 | ||||||
chr16:20475044
|
G | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-318G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475044 | ||||||
chr16:20475046
|
G | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-316G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475046 | ||||||
chr16:20475047
|
A | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-315A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475047 | ||||||
chr16:20475048
|
T | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-314T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475048 | ||||||
chr16:20475049
|
C | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-313C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475049 | ||||||
chr16:20475051
|
A | AG | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-311_895-310ins others(1): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475051 | ||||||
chr16:20475070
|
C | T | 1 | a0010c0012t0001g0052 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.895-292C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475070 | ||||||
chr16:20475317
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.895-45C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 6/13 | chr16 | 20475317 | ||||||
chr16:20475530
|
C | T | 1 | a0004c0004t0002g0312 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.974+89C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/13 | chr16 | 20475530 | ||||||
chr16:20475583
|
C | A | 1 | a0003c0003t0003g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.975-67C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/13 | chr16 | 20475583 | ||||||
chr16:20475591
|
G | T | 53 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(50): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.975-59G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 7/13 | chr16 | 20475591 | ||||||
chr16:20475792
|
A | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | HG01891.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+19A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475792 | ||||||
chr16:20475803
|
T | G | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1098+30T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475803 | ||||||
chr16:20475875
|
C | T | 1 | a0004c0004t0002g0313 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1098+102C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475875 | ||||||
chr16:20475891
|
A | G | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1098+118A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475891 | ||||||
chr16:20475893
|
C | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1098+120C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475893 | ||||||
chr16:20475930
|
C | A | 2 | a0002c0002t0003g0214a0006c0006t0002g0348 | 2 | NA18942.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1098+157C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20475930 | ||||||
chr16:20476001
|
A | C | 5 | a0003c0003t0002g0173a0003c0003t0002g0174a0003c0003t0005g0031others(2): Show | 6 | HG01168.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+228A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476001 | ||||||
chr16:20476068
|
C | G | 17 | a0003c0003t0007g0011a0003c0003t0007g0249a0003c0010t0001g0158others(14): Show | 20 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098+295C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476068 | ||||||
chr16:20476182
|
A | G | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1098+409A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476182 | ||||||
chr16:20476243
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+470A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476243 | ||||||
chr16:20476405
|
C | T | 1 | a0003c0003t0003g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1098+632C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476405 | ||||||
chr16:20476477
|
C | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1098+704C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476477 | ||||||
chr16:20476540
|
T | C | 1 | a0002c0002t0003g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1098+767T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476540 | ||||||
chr16:20476700
|
G | A | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1099-669G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476700 | ||||||
chr16:20476700
|
G | T | 1 | a0003c0003t0005g0285 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099-669G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476700 | ||||||
chr16:20476785
|
C | A | 159 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(156): Show | 180 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1099-584C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476785 | ||||||
chr16:20476793
|
T | C | 1 | a0004c0004t0002g0330 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1099-576T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476793 | ||||||
chr16:20476997
|
T | C | 1 | a0021c0025t0005g0291 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099-372T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20476997 | ||||||
chr16:20477047
|
C | T | 234 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(231): Show | 262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1099-322C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477047 | ||||||
chr16:20477125
|
G | A | 8 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(5): Show | 8 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-244G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477125 | ||||||
chr16:20477198
|
G | T | 1 | a0005c0005t0001g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1099-171G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477198 | ||||||
chr16:20477289
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1099-80T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 8/13 | chr16 | 20477289 | ||||||
chr16:20477473
|
G | A | 2 | a0003c0003t0003g0251a0003c0003t0003g0252 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1179+24G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477473 | ||||||
chr16:20477481
|
T | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1179+32T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477481 | ||||||
chr16:20477577
|
A | G | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+128A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477577 | ||||||
chr16:20477639
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1179+190T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477639 | ||||||
chr16:20477708
|
T | C | 1 | a0003c0003t0002g0340 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1179+259T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477708 | ||||||
chr16:20477812
|
C | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+363C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477812 | ||||||
chr16:20477880
|
T | C | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1179+431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477880 | ||||||
chr16:20477943
|
C | T | 1 | a0006c0006t0003g0359 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1179+494C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477943 | ||||||
chr16:20477957
|
C | T | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+508C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20477957 | ||||||
chr16:20478047
|
T | G | 6 | a0006c0006t0002g0348a0006c0006t0002g0349a0006c0006t0002g0365others(3): Show | 8 | NA18942.hp2 NA18949.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-529T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478047 | ||||||
chr16:20478195
|
C | A | 235 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(232): Show | 263 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1180-381C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478195 | ||||||
chr16:20478252
|
G | C | 221 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(218): Show | 248 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1180-324G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478252 | ||||||
chr16:20478280
|
G | A | 11 | a0003c0003t0002g0305a0003c0003t0002g0306a0003c0003t0002g0307others(8): Show | 12 | NA18943.hp2 NA18945.hp1 NA18971.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-296G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478280 | ||||||
chr16:20478332
|
G | A | 55 | a0003c0003t0002g0034a0003c0003t0002g0037a0003c0003t0002g0272others(52): Show | 59 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.1180-244G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478332 | ||||||
chr16:20478409
|
C | T | 1 | a0001c0001t0025g0055 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1180-167C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478409 | ||||||
chr16:20478546
|
A | C | 53 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(50): Show | 59 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1180-30A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478546 | ||||||
chr16:20478546
|
A | G | 1 | a0003c0003t0002g0308 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1180-30A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 9/13 | chr16 | 20478546 | ||||||
chr16:20478693
|
C | T | 2 | a0003c0003t0005g0175a0003c0003t0005g0176 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1281+16C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478693 | ||||||
chr16:20478733
|
G | A | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+56G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478733 | ||||||
chr16:20478746
|
A | C | 67 | a0003c0003t0002g0033a0003c0003t0002g0294a0003c0003t0002g0305others(64): Show | 74 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1281+69A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478746 | ||||||
chr16:20478793
|
C | G | 2 | a0002c0002t0003g0260a0003c0003t0002g0250 | 2 | NA18747.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1281+116C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478793 | ||||||
chr16:20478954
|
T | C | 1 | a0002c0002t0008g0207 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1281+277T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20478954 | ||||||
chr16:20479026
|
C | A | 1 | a0004c0004t0002g0335 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1281+349C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479026 | ||||||
chr16:20479035
|
A | G | 3 | a0003c0003t0002g0033a0004c0004t0002g0326a0004c0004t0002g0327 | 4 | HG02698.hp2 HG03490.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+358A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479035 | ||||||
chr16:20479049
|
G | T | 2 | a0006c0006t0002g0348a0006c0006t0002g0349 | 2 | NA18942.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1281+372G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479049 | ||||||
chr16:20479291
|
C | T | 220 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(217): Show | 247 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1281+614C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479291 | ||||||
chr16:20479305
|
A | T | 1 | a0004c0004t0002g0318 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1281+628A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479305 | ||||||
chr16:20479336
|
T | C | 234 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(231): Show | 262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1281+659T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479336 | ||||||
chr16:20479389
|
A | C | 1 | a0004c0004t0002g0322 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1281+712A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479389 | ||||||
chr16:20479400
|
A | C | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+723A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479400 | ||||||
chr16:20479406
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | NA19060.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1281+729G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479406 | ||||||
chr16:20479417
|
C | T | 2 | a0009c0009t0006g0154a0009c0009t0006g0165 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1281+740C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479417 | ||||||
chr16:20479447
|
T | A | 2 | a0002c0002t0003g0240a0012c0013t0002g0236 | 2 | HG00408.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1281+770T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479447 | ||||||
chr16:20479575
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1281+898T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479575 | ||||||
chr16:20479661
|
G | A | 14 | a0003c0010t0001g0158a0003c0010t0001g0159a0003c0010t0001g0161others(11): Show | 15 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-912G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479661 | ||||||
chr16:20479675
|
T | A | 160 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(157): Show | 181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1282-898T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479675 | ||||||
chr16:20479730
|
A | C | 1 | a0004c0004t0002g0304 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1282-843A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479730 | ||||||
chr16:20479736
|
C | T | 234 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(231): Show | 262 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1282-837C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479736 | ||||||
chr16:20479772
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1282-801A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479772 | ||||||
chr16:20479890
|
C | A | 1 | a0002c0002t0003g0215 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1282-683C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479890 | ||||||
chr16:20479906
|
G | A | 2 | a0002c0002t0003g0237a0004c0004t0002g0304 | 2 | HG03710.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1282-667G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20479906 | ||||||
chr16:20480035
|
C | A | 1 | a0002c0002t0003g0216 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1282-538C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480035 | ||||||
chr16:20480099
|
C | T | 1 | a0003c0003t0002g0250 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1282-474C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480099 | ||||||
chr16:20480201
|
T | G | 1 | a0003c0010t0001g0158 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1282-372T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480201 | ||||||
chr16:20480235
|
A | G | 1 | a0005c0005t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1282-338A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480235 | ||||||
chr16:20480244
|
G | A | 160 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(157): Show | 181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1282-329G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480244 | ||||||
chr16:20480285
|
T | C | 1 | a0003c0026t0007g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1282-288T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480285 | ||||||
chr16:20480375
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1282-198A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480375 | ||||||
chr16:20480397
|
G | A | 1 | a0001c0001t0004g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1282-176G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480397 | ||||||
chr16:20480572
|
G | T | 1 | a0004c0004t0002g0293 | 1 | NA19062.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1282-1G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 10/13 | chr16 | 20480572 | ||||||
chr16:20480761
|
C | G | 1 | a0019c0024t0002g0311 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1409+61C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/13 | chr16 | 20480761 | ||||||
chr16:20480765
|
T | C | 2 | a0003c0015t0001g0150a0003c0015t0001g0151 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1410-57T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 11/13 | chr16 | 20480765 | ||||||
chr16:20480928
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01891.hp2 | splice_region_variant&intron_variant | LOW | c.1509+7G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480928 | ||||||
chr16:20480954
|
C | G | 6 | a0009c0009t0001g0167a0009c0009t0006g0023a0009c0009t0006g0154others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+33C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480954 | ||||||
chr16:20480977
|
G | A | 1 | a0016c0028t0001g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1509+56G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480977 | ||||||
chr16:20480982
|
A | T | 236 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(233): Show | 264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1509+61A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480982 | ||||||
chr16:20480985
|
G | A | 236 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(233): Show | 264 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1509+64G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480985 | ||||||
chr16:20480994
|
C | T | 238 | a0002c0002t0002g0199a0002c0002t0002g0204a0002c0002t0002g0219others(235): Show | 266 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1509+73C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20480994 | ||||||
chr16:20481065
|
C | T | 54 | a0002c0002t0008g0209a0003c0003t0002g0033a0003c0003t0002g0294others(51): Show | 60 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1509+144C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481065 | ||||||
chr16:20481069
|
C | T | 1 | a0001c0001t0004g0113 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1509+148C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481069 | ||||||
chr16:20481077
|
C | T | 2 | a0005c0005t0001g0063a0005c0005t0001g0078 | 2 | HG02083.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1509+156C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481077 | ||||||
chr16:20481097
|
C | T | 1 | a0002c0002t0008g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+176C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481097 | ||||||
chr16:20481098
|
C | T | 1 | a0002c0002t0008g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+177C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481098 | ||||||
chr16:20481125
|
A | T | 1 | a0004c0004t0002g0293 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1509+204A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481125 | ||||||
chr16:20481174
|
A | C | 12 | a0001c0001t0001g0155a0001c0001t0006g0090a0002c0002t0008g0209others(9): Show | 13 | HG01884.hp2 HG01934.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1509+253A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481174 | ||||||
chr16:20481199
|
C | T | 2 | a0002c0002t0008g0209a0003c0003t0002g0282 | 2 | NA19043.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1509+278C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481199 | ||||||
chr16:20481250
|
A | G | 1 | a0002c0002t0008g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+329A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481250 | ||||||
chr16:20481257
|
G | A | 1 | a0002c0002t0008g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+336G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481257 | ||||||
chr16:20481266
|
C | T | 1 | a0002c0002t0008g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1509+345C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481266 | ||||||
chr16:20481269
|
A | G | 1 | a0002c0002t0014g0025 | 2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1509+348A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481269 | ||||||
chr16:20481278
|
G | T | 6 | a0002c0002t0008g0209a0003c0003t0002g0173a0003c0003t0002g0174others(3): Show | 6 | HG03831.hp1 NA18522.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+357G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481278 | ||||||
chr16:20481331
|
G | A | 9 | a0002c0002t0003g0213a0002c0002t0003g0218a0002c0002t0008g0209others(6): Show | 9 | HG02559.hp1 HG02970.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1509+410G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481331 | ||||||
chr16:20481333
|
G | T | 1 | a0004c0004t0002g0293 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1509+412G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481333 | ||||||
chr16:20481386
|
T | C | 7 | a0002c0002t0003g0213a0002c0002t0003g0218a0003c0003t0002g0173others(4): Show | 7 | HG02630.hp2 HG03831.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+465T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481386 | ||||||
chr16:20481387
|
G | A | 7 | a0002c0002t0003g0213a0002c0002t0003g0218a0003c0003t0002g0173others(4): Show | 7 | HG02630.hp2 HG03831.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+466G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481387 | ||||||
chr16:20481388
|
T | C | 1 | a0003c0003t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1509+467T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481388 | ||||||
chr16:20481398
|
A | G | 9 | a0002c0002t0003g0213a0002c0002t0003g0218a0003c0003t0002g0173others(6): Show | 9 | HG02258.hp1 HG02630.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+477A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481398 | ||||||
chr16:20481424
|
T | G | 1 | a0010c0012t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1509+503T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481424 | ||||||
chr16:20481452
|
C | G | 214 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0081others(211): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1509+531C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481452 | ||||||
chr16:20481458
|
T | C | 7 | a0001c0001t0006g0090a0009c0009t0001g0167a0009c0009t0006g0023others(4): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1509+537T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481458 | ||||||
chr16:20481474
|
A | AG | 67 | a0001c0001t0006g0090a0003c0003t0002g0277a0003c0003t0002g0282others(64): Show | 73 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1509+553_1509+554i others(3): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481474 | ||||||
chr16:20481486
|
G | A | 68 | a0001c0001t0006g0090a0003c0003t0002g0282a0003c0003t0002g0294others(65): Show | 74 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1509+565G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481486 | ||||||
chr16:20481500
|
G | A | 169 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0180others(166): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1509+579G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481500 | ||||||
chr16:20481507
|
T | A | 181 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0180others(178): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1509+586T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481507 | ||||||
chr16:20481518
|
C | T | 70 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0089others(67): Show | 77 | HG00673.hp2 HG01168.hp2 HG01169.hp1 others(74): Show |
intron_variant | MODIFIER | c.1509+597C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481518 | ||||||
chr16:20481590
|
G | A | 7 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0285others(4): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+669G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481590 | ||||||
chr16:20481618
|
G | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0066a0002c0002t0003g0239others(27): Show | 32 | HG00741.hp1 HG01123.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1509+697G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481618 | ||||||
chr16:20481621
|
G | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0066a0002c0002t0003g0239others(27): Show | 32 | HG00741.hp1 HG01123.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1509+700G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481621 | ||||||
chr16:20481629
|
T | TTAGA | 4 | a0003c0003t0003g0202a0003c0003t0003g0252a0003c0003t0003g0253others(1): Show | 4 | HG00741.hp1 HG01361.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+711_1509+712i others(6): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20481629 | |||||
chr16:20481633
|
C | A | 4 | a0003c0003t0003g0202a0003c0003t0003g0252a0003c0003t0003g0253others(1): Show | 4 | HG00741.hp1 HG01361.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+712C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481633 | ||||||
chr16:20481640
|
A | G | 2 | a0002c0002t0003g0230a0002c0002t0003g0231 | 2 | NA18989.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1509+719A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481640 | ||||||
chr16:20481642
|
G | A | 3 | a0003c0003t0003g0202a0003c0003t0003g0252a0003c0003t0003g0253 | 3 | HG00741.hp1 HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1509+721G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481642 | ||||||
chr16:20481660
|
A | C | 11 | a0001c0001t0006g0090a0001c0001t0026g0061a0003c0003t0002g0277others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1509+739A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481660 | ||||||
chr16:20481674
|
A | G | 98 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0168others(95): Show | 106 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1509+753A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481674 | ||||||
chr16:20481685
|
C | T | 1 | a0003c0003t0002g0342 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1509+764C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481685 | ||||||
chr16:20481773
|
A | C | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1509+852A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481773 | ||||||
chr16:20481774
|
C | A | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1509+853C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481774 | ||||||
chr16:20481829
|
G | T | 2 | a0004c0004t0002g0279a0008c0008t0001g0146 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1509+908G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481829 | ||||||
chr16:20481859
|
A | T | 1 | a0002c0002t0003g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1509+938A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481859 | ||||||
chr16:20481876
|
T | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(297): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1509+955T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481876 | ||||||
chr16:20481902
|
C | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(189): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1509+981C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481902 | ||||||
chr16:20481976
|
A | C | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1509+1055A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481976 | ||||||
chr16:20481997
|
T | C | 282 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(279): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1510-1061T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20481997 | ||||||
chr16:20482053
|
T | G | 2 | a0002c0002t0007g0241a0003c0026t0007g0170 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-1005T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482053 | ||||||
chr16:20482071
|
T | G | 2 | a0002c0002t0007g0241a0003c0026t0007g0170 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-987T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482071 | ||||||
chr16:20482084
|
G | A | 2 | a0006c0006t0002g0270a0017c0030t0031g0122 | 2 | HG01928.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1510-974G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482084 | ||||||
chr16:20482091
|
T | C | 16 | a0001c0001t0006g0090a0003c0003t0002g0371a0003c0003t0007g0271others(13): Show | 17 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1510-967T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482091 | ||||||
chr16:20482093
|
C | A | 8 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0175others(5): Show | 10 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1510-965C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482093 | ||||||
chr16:20482095
|
C | T | 16 | a0001c0001t0006g0090a0003c0003t0002g0371a0003c0003t0007g0271others(13): Show | 17 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1510-963C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482095 | ||||||
chr16:20482100
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1510-958A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482100 | ||||||
chr16:20482122
|
G | A | 5 | a0002c0002t0007g0241a0003c0003t0007g0011a0003c0003t0007g0249others(2): Show | 7 | HG02055.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510-936G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482122 | ||||||
chr16:20482130
|
G | C | 3 | a0002c0002t0007g0241a0003c0026t0007g0170a0008c0008t0001g0146 | 3 | HG02055.hp2 HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-928G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482130 | ||||||
chr16:20482134
|
C | CA | 23 | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0006g0090others(20): Show | 24 | HG00408.hp2 HG02055.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1510-903dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482134 | |||||
chr16:20482134
|
CA | C | 21 | a0001c0001t0001g0057a0001c0001t0001g0119a0002c0002t0003g0257others(18): Show | 23 | HG00738.hp2 HG01884.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1510-903delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482134 | |||||
chr16:20482134
|
CAA | C | 45 | a0001c0001t0001g0066a0001c0001t0026g0061a0002c0002t0002g0204others(42): Show | 49 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510-904_1510-903d others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482134 | |||||
chr16:20482152
|
A | G | 2 | a0003c0003t0007g0011a0003c0003t0007g0249 | 4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-906A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482152 | ||||||
chr16:20482164
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1510-894A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482164 | ||||||
chr16:20482169
|
A | C | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510-889A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482169 | ||||||
chr16:20482170
|
G | GA | 6 | a0003c0003t0002g0272a0003c0003t0002g0345a0003c0003t0002g0371others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1510-881dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20482170 | |||||
chr16:20482271
|
G | A | 3 | a0004c0004t0002g0295a0007c0007t0001g0082a0021c0025t0005g0291 | 3 | HG02451.hp1 HG03540.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1510-787G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482271 | ||||||
chr16:20482289
|
G | T | 1 | a0004c0004t0002g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1510-769G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482289 | ||||||
chr16:20482295
|
C | T | 1 | a0004c0004t0002g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1510-763C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482295 | ||||||
chr16:20482305
|
A | C | 1 | a0009c0009t0001g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1510-753A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482305 | ||||||
chr16:20482340
|
G | C | 1 | a0003c0003t0005g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1510-718G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482340 | ||||||
chr16:20482356
|
G | A | 1 | a0003c0003t0005g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1510-702G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482356 | ||||||
chr16:20482388
|
T | A | 1 | a0004c0004t0002g0293 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1510-670T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482388 | ||||||
chr16:20482399
|
G | C | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510-659G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482399 | ||||||
chr16:20482400
|
C | G | 19 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(16): Show | 22 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1510-658C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482400 | ||||||
chr16:20482470
|
G | A | 1 | a0002c0002t0003g0260 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1510-588G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482470 | ||||||
chr16:20482594
|
T | A | 61 | a0003c0003t0007g0011a0003c0003t0007g0249a0004c0004t0002g0003others(58): Show | 69 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1510-464T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482594 | ||||||
chr16:20482610
|
T | C | 2 | a0004c0004t0002g0322a0008c0008t0001g0181 | 2 | NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1510-448T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482610 | ||||||
chr16:20482665
|
C | T | 2 | a0002c0002t0007g0241a0003c0026t0007g0170 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1510-393C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482665 | ||||||
chr16:20482710
|
C | T | 4 | a0005c0005t0004g0041a0005c0005t0004g0076a0005c0005t0004g0077others(1): Show | 4 | NA18964.hp1 NA18982.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-348C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482710 | ||||||
chr16:20482790
|
C | T | 1 | a0001c0017t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1510-268C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482790 | ||||||
chr16:20482791
|
T | A | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510-267T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482791 | ||||||
chr16:20482815
|
T | C | 1 | a0002c0002t0003g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1510-243T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482815 | ||||||
chr16:20482823
|
T | C | 4 | a0003c0003t0005g0176a0011c0011t0005g0274a0011c0011t0005g0275others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-235T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482823 | ||||||
chr16:20482861
|
T | C | 1 | a0002c0002t0003g0377 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1510-197T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482861 | ||||||
chr16:20482946
|
G | C | 1 | a0004c0004t0002g0337 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1510-112G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482946 | ||||||
chr16:20482957
|
G | T | 1 | a0002c0002t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1510-101G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482957 | ||||||
chr16:20482974
|
G | C | 2 | a0003c0003t0007g0011a0003c0003t0007g0249 | 4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-84G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20482974 | ||||||
chr16:20483014
|
T | C | 48 | a0001c0001t0001g0066a0001c0001t0001g0128a0001c0001t0026g0061others(45): Show | 50 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.1510-44T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 12/13 | chr16 | 20483014 | ||||||
chr16:20483257
|
G | C | 18 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(15): Show | 21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1629+80G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483257 | ||||||
chr16:20483263
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+86T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483263 | ||||||
chr16:20483265
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+88C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483265 | ||||||
chr16:20483287
|
T | TG | 19 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(16): Show | 22 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1629+112dupG | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483287 | |||||
chr16:20483291
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+114T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483291 | ||||||
chr16:20483294
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+117G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483294 | ||||||
chr16:20483296
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+119G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483296 | ||||||
chr16:20483300
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+123C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483300 | ||||||
chr16:20483301
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+124A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483301 | ||||||
chr16:20483305
|
C | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+128C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483305 | ||||||
chr16:20483308
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+131G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483308 | ||||||
chr16:20483313
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+136T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483313 | ||||||
chr16:20483330
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+153G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483330 | ||||||
chr16:20483335
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+158T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483335 | ||||||
chr16:20483336
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+159G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483336 | ||||||
chr16:20483342
|
G | A | 1 | a0002c0002t0003g0237 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1629+165G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483342 | ||||||
chr16:20483358
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+181T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483358 | ||||||
chr16:20483372
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+195T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483372 | ||||||
chr16:20483385
|
C | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+208C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483385 | ||||||
chr16:20483391
|
GA | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1629+217delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483391 | |||||
chr16:20483399
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+222A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483399 | ||||||
chr16:20483427
|
C | T | 19 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(16): Show | 22 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1629+250C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483427 | ||||||
chr16:20483485
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+308A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483485 | ||||||
chr16:20483488
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+311T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483488 | ||||||
chr16:20483503
|
G | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+326G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483503 | ||||||
chr16:20483512
|
G | A | 1 | a0002c0002t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1629+335G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483512 | ||||||
chr16:20483524
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+347T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483524 | ||||||
chr16:20483525
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+348G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483525 | ||||||
chr16:20483538
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+361G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483538 | ||||||
chr16:20483544
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+367C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483544 | ||||||
chr16:20483546
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+369G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483546 | ||||||
chr16:20483562
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+385T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483562 | ||||||
chr16:20483569
|
C | CA | 15 | a0001c0001t0010g0048a0002c0002t0003g0197a0002c0002t0003g0224others(12): Show | 16 | HG00673.hp2 HG01074.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1629+425dupA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
C | CAA | 44 | a0001c0001t0004g0126a0001c0001t0010g0044a0001c0001t0010g0045others(41): Show | 50 | HG00280.hp2 HG00408.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1629+424_1629+425d others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
C | CAAA | 53 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0049others(50): Show | 65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1629+423_1629+425d others(5): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
C | CAAAA | 60 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0050others(57): Show | 65 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1629+422_1629+425d others(6): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
C | CAAAAA | 46 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 57 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1629+421_1629+425d others(7): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
C | CAAAAAA | 13 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0088others(10): Show | 16 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1629+420_1629+425d others(8): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
C | CAAAAAAA | 11 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0149others(8): Show | 11 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1629+419_1629+425d others(9): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CA | C | 20 | a0001c0001t0001g0128a0001c0001t0004g0111a0002c0002t0002g0204others(17): Show | 21 | HG00639.hp1 HG02056.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1629+425delA | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CAA | C | 20 | a0003c0003t0002g0355a0004c0004t0002g0269a0004c0004t0002g0279others(17): Show | 20 | HG01978.hp1 HG02129.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.1629+424_1629+425d others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CAAA | C | 37 | a0002c0002t0007g0241a0004c0004t0002g0003a0004c0004t0002g0032others(34): Show | 43 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1629+423_1629+425d others(5): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CAAAAAAA | C | 11 | a0001c0001t0006g0090a0003c0003t0007g0271a0003c0010t0006g0163others(8): Show | 12 | HG02055.hp1 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1629+419_1629+425d others(9): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0060a0001c0017t0001g0064a0001c0017t0001g0065others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+414_1629+425d others(14): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CAAAAAAA others(7): Show |
C | 8 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0175others(5): Show | 10 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1629+412_1629+425d others(16): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483569
|
CAAAAAAA others(10): Show |
C | 4 | a0003c0003t0005g0176a0011c0011t0005g0274a0011c0011t0005g0275others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1629+409_1629+425d others(19): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483569 | |||||
chr16:20483577
|
A | AAAACCAA others(14): Show |
1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+403_1629+404i others(23): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20483577 | |||||
chr16:20483589
|
A | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+412A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483589 | ||||||
chr16:20483600
|
A | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+423A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483600 | ||||||
chr16:20483603
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+426G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483603 | ||||||
chr16:20483608
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+431T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483608 | ||||||
chr16:20483614
|
A | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+437A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483614 | ||||||
chr16:20483650
|
C | G | 3 | a0003c0003t0002g0277a0003c0003t0002g0288a0007c0007t0001g0082 | 3 | HG02280.hp1 HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1629+473C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483650 | ||||||
chr16:20483686
|
T | C | 2 | a0002c0002t0003g0262a0017c0030t0031g0122 | 2 | HG01928.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1629+509T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483686 | ||||||
chr16:20483701
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+524A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483701 | ||||||
chr16:20483715
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1629+538T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483715 | ||||||
chr16:20483849
|
A | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+672A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483849 | ||||||
chr16:20483856
|
G | A | 3 | a0003c0003t0007g0011a0003c0003t0007g0249a0017c0030t0031g0122 | 5 | HG01928.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+679G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483856 | ||||||
chr16:20483857
|
G | A | 3 | a0003c0003t0007g0011a0003c0003t0007g0249a0017c0030t0031g0122 | 5 | HG01928.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1629+680G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483857 | ||||||
chr16:20483884
|
G | A | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1629+707G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483884 | ||||||
chr16:20483906
|
G | A | 62 | a0002c0002t0007g0241a0003c0003t0007g0011a0003c0003t0007g0249others(59): Show | 70 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1629+729G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483906 | ||||||
chr16:20483906
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1629+729G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483906 | ||||||
chr16:20483907
|
T | A | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1629+730T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483907 | ||||||
chr16:20483910
|
C | A | 63 | a0002c0002t0007g0241a0003c0003t0007g0011a0003c0003t0007g0249others(60): Show | 71 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1629+733C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483910 | ||||||
chr16:20483948
|
T | C | 20 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(17): Show | 23 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1629+771T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483948 | ||||||
chr16:20483983
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1629+806A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20483983 | ||||||
chr16:20484033
|
T | C | 1 | a0002c0002t0003g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1629+856T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484033 | ||||||
chr16:20484091
|
C | G | 18 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(15): Show | 21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1629+914C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484091 | ||||||
chr16:20484140
|
A | T | 1 | a0004c0004t0002g0293 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1629+963A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484140 | ||||||
chr16:20484202
|
G | C | 13 | a0001c0001t0001g0155a0001c0001t0006g0090a0003c0003t0007g0271others(10): Show | 14 | HG01884.hp2 HG01928.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1629+1025G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484202 | ||||||
chr16:20484216
|
C | T | 1 | a0003c0003t0003g0252 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1629+1039C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484216 | ||||||
chr16:20484218
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1629+1041T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484218 | ||||||
chr16:20484230
|
G | T | 2 | a0003c0003t0007g0011a0003c0003t0007g0249 | 4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1629+1053G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484230 | ||||||
chr16:20484239
|
C | T | 5 | a0001c0001t0001g0060a0001c0017t0001g0064a0001c0017t0001g0065others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+1062C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484239 | ||||||
chr16:20484341
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1629+1164G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484341 | ||||||
chr16:20484413
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1236C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484413 | ||||||
chr16:20484504
|
C | G | 13 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0175others(10): Show | 15 | HG01884.hp1 HG01928.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1629+1327C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484504 | ||||||
chr16:20484514
|
T | C | 1 | a0005c0005t0004g0074 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1629+1337T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484514 | ||||||
chr16:20484555
|
C | T | 2 | a0003c0003t0012g0171a0003c0003t0012g0172 | 2 | HG03831.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1629+1378C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484555 | ||||||
chr16:20484723
|
GT | G | 14 | a0001c0001t0006g0090a0003c0003t0007g0271a0003c0003t0012g0171others(11): Show | 15 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1629+1548delT | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20484723 | |||||
chr16:20484761
|
T | C | 1 | a0004c0004t0002g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1629+1584T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484761 | ||||||
chr16:20484764
|
A | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1587A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484764 | ||||||
chr16:20484785
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1608A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484785 | ||||||
chr16:20484824
|
C | A | 3 | a0003c0003t0002g0294a0003c0003t0002g0306a0003c0003t0002g0331 | 3 | NA18971.hp1 NA18998.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1629+1647C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484824 | ||||||
chr16:20484838
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1661C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484838 | ||||||
chr16:20484854
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1677T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484854 | ||||||
chr16:20484857
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1680T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484857 | ||||||
chr16:20484859
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1682T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484859 | ||||||
chr16:20484860
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1683T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484860 | ||||||
chr16:20484868
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1691C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484868 | ||||||
chr16:20484869
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1692A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484869 | ||||||
chr16:20484874
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1629+1697G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484874 | ||||||
chr16:20484906
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1668C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484906 | ||||||
chr16:20484951
|
A | G | 78 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(75): Show | 87 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1630-1623A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484951 | ||||||
chr16:20484960
|
C | T | 2 | a0004c0004t0002g0324a0004c0004t0002g0330 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1630-1614C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484960 | ||||||
chr16:20484988
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1586T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484988 | ||||||
chr16:20484998
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1576G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20484998 | ||||||
chr16:20485012
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1562G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485012 | ||||||
chr16:20485019
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1555A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485019 | ||||||
chr16:20485032
|
A | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1542A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485032 | ||||||
chr16:20485069
|
TGTTACCC others(130): Show |
T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1503_1630-136 others(4): Show |
ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 20485069 | |||||
chr16:20485210
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1364T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485210 | ||||||
chr16:20485211
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1363G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485211 | ||||||
chr16:20485238
|
G | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1336G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485238 | ||||||
chr16:20485258
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1316C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485258 | ||||||
chr16:20485343
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1231G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485343 | ||||||
chr16:20485357
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1217T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485357 | ||||||
chr16:20485369
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1205C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485369 | ||||||
chr16:20485413
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1161G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485413 | ||||||
chr16:20485485
|
C | T | 14 | a0001c0001t0006g0090a0003c0003t0007g0271a0003c0003t0012g0171others(11): Show | 15 | HG01928.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1630-1089C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485485 | ||||||
chr16:20485490
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1084C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485490 | ||||||
chr16:20485507
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1067T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485507 | ||||||
chr16:20485523
|
T | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1051T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485523 | ||||||
chr16:20485549
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-1025T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485549 | ||||||
chr16:20485591
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-983G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485591 | ||||||
chr16:20485601
|
G | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-973G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485601 | ||||||
chr16:20485610
|
T | A | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1630-964T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485610 | ||||||
chr16:20485614
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-960T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485614 | ||||||
chr16:20485616
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-958A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485616 | ||||||
chr16:20485638
|
T | G | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1630-936T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485638 | ||||||
chr16:20485645
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-929C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485645 | ||||||
chr16:20485646
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-928A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485646 | ||||||
chr16:20485648
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1630-926G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485648 | ||||||
chr16:20485668
|
C | G | 4 | a0008c0008t0001g0190a0012c0013t0002g0229a0017c0030t0031g0122others(1): Show | 4 | HG01928.hp2 NA18612.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-906C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485668 | ||||||
chr16:20485670
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1630-904T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485670 | ||||||
chr16:20485691
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-883C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485691 | ||||||
chr16:20485703
|
A | C | 5 | a0003c0003t0005g0176a0011c0011t0005g0274a0011c0011t0005g0275others(2): Show | 5 | HG01928.hp2 HG02145.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1630-871A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485703 | ||||||
chr16:20485804
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-770G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485804 | ||||||
chr16:20485805
|
G | T | 17 | a0001c0001t0006g0090a0002c0002t0007g0241a0003c0003t0007g0011others(14): Show | 20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1630-769G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485805 | ||||||
chr16:20485823
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-751A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485823 | ||||||
chr16:20485833
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-741A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485833 | ||||||
chr16:20485835
|
C | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-739C>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485835 | ||||||
chr16:20485836
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-738A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485836 | ||||||
chr16:20485843
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-731C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485843 | ||||||
chr16:20485849
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-725G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485849 | ||||||
chr16:20485866
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-708T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485866 | ||||||
chr16:20485890
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-684A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485890 | ||||||
chr16:20485895
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-679C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485895 | ||||||
chr16:20485897
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-677C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485897 | ||||||
chr16:20485925
|
A | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-649A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485925 | ||||||
chr16:20485951
|
A | G | 52 | a0001c0001t0001g0066a0001c0001t0001g0128a0001c0001t0026g0061others(49): Show | 54 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630-623A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485951 | ||||||
chr16:20485969
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-605T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485969 | ||||||
chr16:20485992
|
T | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-582T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485992 | ||||||
chr16:20485998
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-576G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20485998 | ||||||
chr16:20486057
|
T | A | 51 | a0001c0001t0001g0066a0001c0001t0001g0128a0001c0001t0026g0061others(48): Show | 53 | HG00673.hp2 HG01258.hp1 HG01891.hp1 others(50): Show |
intron_variant | MODIFIER | c.1630-517T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486057 | ||||||
chr16:20486066
|
G | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-508G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486066 | ||||||
chr16:20486089
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-485C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486089 | ||||||
chr16:20486111
|
A | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-463A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486111 | ||||||
chr16:20486134
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-440G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486134 | ||||||
chr16:20486138
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-436G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486138 | ||||||
chr16:20486150
|
T | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-424T>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486150 | ||||||
chr16:20486150
|
T | G | 384 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(381): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.1630-424T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486150 | ||||||
chr16:20486164
|
T | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-410T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486164 | ||||||
chr16:20486190
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-384A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486190 | ||||||
chr16:20486223
|
T | G | 1 | a0002c0002t0003g0238 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1630-351T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486223 | ||||||
chr16:20486251
|
T | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1630-323T>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486251 | ||||||
chr16:20486268
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-306T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486268 | ||||||
chr16:20486294
|
A | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-280A>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486294 | ||||||
chr16:20486323
|
C | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-251C>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486323 | ||||||
chr16:20486350
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-224T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486350 | ||||||
chr16:20486355
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-219T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486355 | ||||||
chr16:20486366
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-208G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486366 | ||||||
chr16:20486377
|
A | C | 1 | a0020c0027t0020g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1630-197A>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486377 | ||||||
chr16:20486378
|
G | T | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-196G>T | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486378 | ||||||
chr16:20486414
|
C | G | 2 | a0003c0003t0007g0011a0003c0003t0007g0249 | 4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630-160C>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486414 | ||||||
chr16:20486430
|
T | C | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-144T>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486430 | ||||||
chr16:20486453
|
G | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1630-121G>C | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486453 | ||||||
chr16:20486457
|
A | G | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-117A>G | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486457 | ||||||
chr16:20486461
|
G | A | 1 | a0017c0030t0031g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1630-113G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486461 | ||||||
chr16:20486533
|
G | A | 3 | a0002c0002t0007g0241a0003c0026t0007g0170a0017c0030t0031g0122 | 3 | HG01928.hp2 HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1630-41G>A | ACSM2A | ENSG00000183747.12 | transcript | ENST00000573854.6 | protein_coding | 13/13 | chr16 | 20486533 |